Hetaryl-substituted benzyl phenyl ethers, method for the production thereof, and their use for combating harmful fungi and animal pests

ABSTRACT

The invention relates to hetaryl-substituted benzyl phenyl ethers of formula (I) in which the substituents have the following meanings: (Q):                    
     C(═CHOCH 3 )—COOCH 3 , C(═CHCH 3 )—COOCH 3 , C(═NOCH 3 )—COOCH 3 , C(═NOCH 3 )—CONHCH 3 , N(—OCH 3 )—COOCH 3  or a group F, G, H or J, whereby # characterizes the bond with the phenyl ring, and (X) five-linked heteroaryl which is optionally substituted by a group Y 2   p  and which contains one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom. The invention also relates to the salts of the inventive hetaryl-substituted benzyl phenyl ethers, to the production of compounds (I), and to the use of compounds (I) for combating harmful fungi and animal pests.

The present invention relates to hetaryl-substituted benzyl phenyl ethers of the formula I

where:

Q is C(═CHOCH₃)—COOCH₃, C(═CHCH₃)—COOCH₃, C(═NOCH₃)—COOCH₃, C(═NOCH₃)—CONHCH₃, N(—OCH₃)—COOCH₃ or

 a group F, G, H, or J

 where

# denotes the bond with the phenyl ring and

R^(A) is hydrogen, cyano, halogen,

 C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₃-C₆-cycloalkyloxy, C₃-C₆-halocycloalkyloxy, C₂-C₆-alkenyloxy, C₂-C₆-haloalkenyloxy, C₂-C₆-alkynyloxy, C₂-C₆-haloalkynyloxy, acetyloxy,

 C₁-C₆-alkylthio, C₁-C₆-haloalkylthio, C₃-C₆-cycloalkylthio, C₂-C₆-alkenylthio, C₂-C₆-haloalkenylthio, C₂-C₆-alkynylthio, C₂-C₆-haloalkynylthio, C₁-C₆-alkylsulfinyl, C₁-C₆-haloalkylsulfinyl, C₃-C₆-cycloalkylsulfinyl, C₂-C₆-alkenylsulfinyl, C₂-C₆-haloalkenylsulfinyl, C₂-C₆-alkynylsulfinyl, C₂-C₆-haloalkynylsulfinyl, C₁-C₆-alkylsulfonyl, C₁-C₆-haloalkylsulfonyl, C₃-C₆-cycloalkylsulfonyl, C₂-C₆-alkenylsulfonyl, C₂-C₆-haloalkenylsulfonyl, C₂-C₆-alkynylsulfonyl, C₂-C₆-haloalkynylsulfonyl,

 amino, C₁-C₆-alkylamino, C₁-C₆-dialkylamino, C₁-C₆-alkoxyamino, (C₁-C₆-alkyl) (C₁-C₆-alkoxy)amino, or

 unsubstituted heterocyclyl or heterocyclyl which is substituted by one to three groups R⁴;

R^(B) is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl or C₂-C₆-haloalkynyl;

R^(C) is hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C₃-C₆-halocycloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₂-C₆-haloalkynyl, hydroxyl, C₁-C₂-alkoxy, acetyloxy, C₂-C₄-alkylcarbonyl or C₂-C₄-alkoxycarbonyl;

X is five-membered hetaryl which is unsubstituted or substituted by a group Y² _(p) and contains one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom;

Y, Y¹ are halogen, cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl or C₁-C₄-alkoxy;

Y² is halogen, cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylamino or C₁-C₄-alkylthio, or

 phenyl, phenoxy or benzyl, where the aromatic rings may be partially or fully halogenated or may carry one to three groups R⁴:

R⁴ is halogen, cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, alkyl, haloalkyl, alkenyl, alkenyloxy, alkynyloxy, alkoxy, haloalkoxy, alkylthio, alkylamino, dialkylamio, formyl, alkylcarbonyl, alkylsulfonyl, alkylsulfoxyl, alkoxycarbonyl, alkylcarbonyloxy, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, where the alkyl groups in these radicals contain 1 to 6 carbon atoms and the abovementioned alkenyl or alkynyl groups in these radicals contain 2 to 8 carbon atoms;

 and/or one to three of the following radicals

cycloalkyl, cycloalkoxy, heterocyclyl, heterocyclyloxy, where the cyclic systems contain 3 to 10 ring members; aryl, aryloxy, arylthio, aryl-C₁-C₆-alkoxy, aryl-C₁-C₆-alkyl, hetaryl, hetaryloxy, hetarylthio, where the aryl radicals preferably contain 6 to 10 ring members, the hetaryl radicals 5 or 6 ring members, where the cyclic systems may be partially or fully halogenated or may be substituted by one to three groups R⁵ or by one or two groups R⁶:

R⁵ is halogen, cyano, nitro, hydroxyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkylcarbonyl, C₃-C₆-cycloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-alkylthio, C₁-C₆-alkylamino, di-C₁-C₆-alkylamino, C₂-C₆-alkenyl, C₂-C₆-alkenyloxy, C₃-C₆-alkynyloxy and C₁-C₄-alkylenedioxy which may be halogenated; and

R⁶ is C(═NOR^(d)) -Γ_(l)-R^(d)′, where R^(d) is hydrogen or C₁-C₆-alkyl, Γ is oxygen, sulfur or NR^(d) and l is 0 or 1;

m, n are 0, 1 or 2, where the radicals Y and Y¹ may be different if m or n=2;

p is 0, 1, 2 or 3, where the radicals Y² may be different if p=2 or 3;

and salts thereof.

Additionally, the invention relates to processes for preparing the compounds I and to the use of the compounds I for controlling harmful fungi and animal pests.

Phenoxymethylenephenylacetic acid methyl esters and methyl amides are known from EP-A 253 213, EP-A 254 426, EP-A 251 082, EP-A 278 595, EP-A 280 185, EP-A 299 694, EP-A 386 561, EP-A 398 692 and EP-A 477 631, and the corresponding methoxycarbamates are known from WO-A 93/15046. Hetaryl-substituted phenylacetic acid derivatives are disclosed in EP-A 811 614.

Cyclic amides which carry an ortho-substituted phenyl ring in the position ortho to the amide carbonyl group are disclosed in WO-A 95/14009, WO-A 96/17851, WO-A 96/26191, WO-A 96/36229, WO-A 96/36615, WO-A 96/36616, WO-A 96/38425, WO-A 97/00612, WO-A 97/02255, WO-A 97/05120, WO-A 97/19935, WO-A 98/05652, WO-A 98/20003 and WO-A 98/23155, and JP-A 09/104676 and JP-A 09/208565. Cyclic amides which carry a substituted heterocycle in the position ortho to the amide carbonyl group are disclosed in WO-A 96/36633.

The compounds described in the abovementioned publications are suitable for use as crop protection agents against harmful fungi and in some cases against animal pests.

However, their action is in many cases unsatisfactory.

It is an object of the invention to provide compounds having improved activity.

This object was achieved by the substituted benzyl phenyl ethers of the formula I. Furthermore, intermediates and processes for preparing the compounds I, and also the use of the compounds I and of compositions comprising them for controlling harmful fungi and animal pests, were found. The fungicidal action is preferred.

Compared with the known compounds, the compounds of the formula I have increased activity against harmful fungi and animal pests.

The compounds of the formula I differ from the compounds known from the abovementioned publications by the design of the phenoxy group, which is substituted by five-membered nitrogen heterocycles or heteroaromatics.

The compounds I can be obtained by different routes, and it is immaterial for the synthesis whether the group Q or the phenoxy group E is constructed first.

The bracket } in the formula E denotes the linkage point with the benzyl skeleton in the formula I.

The construction of the group —Q is known, for example, from the publications cited at the outset, and also from the following publications:

EP-A 254 426, EP-A 370 629, EP-A 463 488, EP-A 472 300 and EP-A 513 580.

Thus, for clarity, the term

Q# is used for C(═CHOCH₃)—COOCH₃, C(—CHCH₃)—COOCH₃, C(═NOCH₃)—COOCH₃, N(—OCH₃)—COOCH₃ or the group F, G, H or J, or a suitable precursor thereof, and

L# is used for the phenoxy group E, or a suitable precursor thereof,

in the descriptions of the reactions below.

For compounds of the formulae IF and IH

preference is given to introducing the phenoxy group in the steps in which Q# is nitro or, in the case of IF, is the group F, and, in the case IH, is the group H.

For compounds of the formulae IG and IJ

preference is given to introducing the phenoxy group in the steps in which Q# is the group G and the group J, respectively.

The synthesis of the compounds I is generally carried out by reacting phenols of the formula II with benzyl derivatives of the formula III#.

In the formula III#, L is a nucleofuge leaving group, such as halogen or alkyl- or arylsulfonate, preferably bromine, chlorine, mesylate, tosylate or triflate.

1) This reaction is usually carried out at 0°C. to 180° C., preferably at 20° C. to 60° C., in an inert organic solvent in the presence of a base [cf. EP-A 254 426; EP-A 463 488; WO-A 93/15046; WO-A 95/18789; WO-A 95/29896].

The benzyl compounds III# are known (EP-A 513 580, EP-A 477 631, EP-A 463 488, EP-A 251 082, EP-A 400 417, EP-A 585 751, WO-A 93/15046) or they can be prepared by the methods described in these publications or by the routes outlined below:

For compounds of the formula IF and the corresponding precursors IIIF, the group Q is preferably synthesized by the following route:

The benzyl compounds IIIF# required for preparing the compounds IF in which R^(A) is hydroxyl, alkoxy, haloalkoxy, cycloalkoxy, halocycloalkoxy, alkenyloxy, haloalkenyloxy, alkynyloxy or haloalkynyloxy are known from the literature [cf. WO-A 97/02255], or they can be obtained by the methods of the cited literature. They can be obtained by the following synthesis route:

This route is suitable not only for preparing the benzyl compounds IIIF# but also, in principle, for synthesizing the group F at each stage of the synthesis of the group L#. The group Q is particularly preferably synthesized at the stage of the compounds IIIF1# or IIIF# in which L# is hydrogen.

The isocyanates of the formula IIIF1# are obtainable by known methods from the corresponding nitrobenzene derivatives via reduction and reaction of the resulting anilines with phosgene [cf. WO-A 97/02255].

The benzyl compounds IIIF# required for preparing the compounds IF in which R^(A) is alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, alkynyl or haloalkynyl are known from the literature [cf. WO-A 96/36229], or they can be obtained by the methods of the cited literature. They can be obtained by reacting the carbamates of the formula IIIF2# with orthoesters:

2) This reaction is generally carried out at from 0° C. to 200° C., preferably from 50° C. to 120° C., in an inert organic solvent [cf. J. Org. Chem., 43 (1978), 936].

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane and tetrahydrofuran, nitrites, ketones, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide, particularly preferably dimethylformamide, tetrahydrofuran or toluene. It is also possible to use mixtures of the abovementioned solvents.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of orthoester, based on IIIF2#.

For compounds of the formula IG and the corresponding precursors IIIG, the group Q is preferably synthesized by the following route:

The benzyl compounds IIIG# required for preparing the compounds IG are known from the literature [WO-A 95/14009; WO-A 97/02255], or they are obtainable by the methods of the cited literature. They can be obtained by the following synthesis routes:

These routes are not only suitable for preparing the benzyl compounds IIIG# but, in principle, at each stage of the synthesis of the isoxazolinone group for synthesizing the phenoxy group E. The group Q is particularly preferably synthesized at the stage of the compounds IIIG or IIIG5 in which L# is hydrogen.

Compounds of the formula IIIG in which R^(A) is alkyl are obtained, by the route known from U.S. Pat. No. 4,952,573, from the corresponding phenylacetic esters IIIG4#.

The benzyl compounds IIIH1#-IIIH3# in which L# is a leaving group L and which are required for preparing the compounds IH are known from the literature [cf. WO-A 96/36229].

The tetrazolinone group H can be synthesized by the synthesis route outlined below.

This route is not only suitable for preparing the benzyl compounds IIIH# and IIIH1#/IIIH5# but also, in principle, at each stage of the synthesis of the group L# for synthesizing the tetrazolinone group. The phenoxy group is particularly preferably synthesized at the nitrobenzene stage.

The isocyanates of the formula IIIF1# are obtainable by known methods from the corresponding nitrobenzene derivatives via reduction and reaction of the resulting anilines with phosgene [cf. WO-A 97/02255].

For compounds of the formula IH and the corresponding precursors IIIH, the group Q is preferably synthesized by the following route:

3) The reaction of the isocyanates IIIA1# with the azides IVa is generally carried out at from −10° C. to 200° C., preferably from 20° C. to 140° C., in an inert organic solvent, in the presence or absence of a base or an acid [cf. J. Org. Chem. 45 (1980), 5130; J. Am. Chem. Soc. 81 (1959), 3076; Tetrahedron 31 (1975), 765; J. Org. Chem. 38 (1973), 675].

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, such as methylene chloride, chloroform and chlorobenzene, ethers, nitriles, and also dimethyl sulfoxide, dimethyl formamide and dimethyl acetamide, particularly preferably toluene, xylene, dimethylformamide and chloroform. If the azide IVa employed is liquid, it can also be used as solvent. It is also possible to employ mixtures of the abovementioned solvents.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of IVa, based on IIIF1#.

In the formula IVa, M is a cation from the group consisting of the alkali metals and alkaline earth metals, trialkylsilyl and alkyl. Preference is given to using trimethylsilyl azide.

Compounds of the formula IIIH2# in which R^(B) is C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₃-C₆-cycloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl or C₂-C₆-haloalkynyl are obtained from tetrazolinones of the formula IIIH1# by alkylation. If L# in the formula IIIH2# is the phenoxy group E, the compounds IIIH2# correspond to the compounds IH.

4) The alkylation of the tetrazolinones IIIH1# to give IIIH2# is generally carried out at from −20° C. to 180° C., preferably from 20° C. to 120° C., in an inert organic solvent in the presence of a base [cf. Synth. Commun. 18 (1988),2011; J. Chem. Soc. Chem. Commun., (1987), 735].

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran, nitriles, alcohols, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide, particularly preferably dimethylformamide, tetrahydrofuran, dimethyl sulfoxide, diethyl ether and toluene. It is also possible to employ mixtures of the abovementioned solvents.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal amides, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls, alkylmagnesium halides, and also alkali metal and alkaline earth metal alkoxides and dimethoxymagnesium, furthermore organic bases, for example tertiary amines, pyridine, substituted pyridines and also bicyclic amines. Particular preference is given to sodium hydride, sodium bicarbonate, sodium carbonate and sodium hydroxide and potassium hydroxide.

The bases are generally employed in equimolar amounts or in excess, but they can also be employed in catalytic amounts or, if appropriate, as solvent.

Suitable alkylating agents are, for example, alkyl halides, alkyl sulfonates, alkyl p-toluenesulfonates, alkyl trifluoromethanesulfonates, alcohols, ethers or alkyl p-bromophenylsulfonates, in particular methyl iodide or dimethyl sulfate.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of alkylating agent, based on IIIH1#.

Compounds of the formula IIIH3# in which R^(B) is C₁-C₆-alkylcarbonyl or C₁-C₆-alkoxycarbonyl are obtained from tetrazolinones of the formula IIIH1# by reaction with acylating agents, such as carbonyl halides, carboxylic anhydrides, carboxylic esters or chloroformates.

5) The acylation of the tetrazolinones IIIH1# to give IIIH3# is generally carried out at from −20° C. to 180° C., preferably from 20° C. to 120° C., in an inert organic solvent in the presence of a base [cf. Synth. Commun. 18 (1988), 2011; J. Chem. Soc. Chem. Commun., (1987), 735].

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane and tetrahydrofuran, nitriles, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide, particularly preferably dimethylformamide, tetrahydrofuran, dimethyl sulfoxide, diethyl ether and toluene. It is also possible to employ mixtures of the abovementioned solvents.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal amides, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, furthermore organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, and also bicyclic amines. Particular preference is given to sodium hydride, sodium bicarbonate, sodium carbonate and sodium hydroxide and potassium hydroxide, triethylamine and pyridine.

The bases are generally employed in equimolar amounts or in excess, but they can also be employed in catalytic amounts or, if appropriate, as solvent.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of acylating agent, based on IIIH1#.

The benzyl compounds IIIJ# required for preparing the compounds IJ in which R^(B) is alkyl, haloalkyl, cycloalkyl, alkenyl, haloalkenyl, alkynyl or haloalkynyl are known from the literature [WO-A 96/36229], or they can be obtained by the methods of the cited literature. They can be obtained by the following synthesis route:

6) The alkylation or acylation of the phenylacetic acid derivatives IIIG4# to give IIIJ1# is generally carried out at from −20° C. to 180° C., preferably from 20° C. to 120° C., in an inert organic solvent in the presence of a base, if appropriate under phase-transfer conditions [cf. Houben-Weyl, Vol. 8 (1952), p.600-610; Org. Syntheses 55 (1976), 91; Org. Reactions 9 (1957), 107; Org. Reactions 17 (1969), 155; J. Am. Chem. Soc., 92 (1970), 1397].

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane and tetrahydrofuran, nitriles, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide, particularly preferably dimethylformamide, tetrahydrofuran, dimethyl sulfoxide, diethyl ether and toluene. It is also possible to employ mixtures of the abovementioned solvents.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, alkali metal and alkaline earth metal hydrides, lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal amides, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls, alkylmagnesium halides, and also alkali metal and alkaline earth metal alkoxides and dimethoxymagnesium, furthermore organic bases, for example tertiary amines, pyridine, substituted pyridines and also bicyclic amines. Particular preference is given to sodium hydride, sodium bicarbonate, sodium carbonate and sodium hydroxide and potassium hydroxide.

The bases are generally employed in equimolar amounts or in excess, but it is also possible to employ them in catalytic amounts or, if appropriate, as solvent.

Suitable alkylating agents are, for example, alkyl halides, alkyl sulfonates, alkyl p-toluenesulfonates, alkyl trifluoromethane-sulfonates, alcohols, ethers or alkyl p-bromophenylsulfonates, in particular methyl iodide or dimethyl sulfate.

Suitable acylating agents are, for example, carbonyl halides, carboxylic anhydrides, carboxylic esters or chloroformates.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of alkylating or acylating agent, based on IIIG4#.

7) The acylation of the phenylacetic acid derivatives IIIJ1# with the carboxylic acid derivatives IVb is generally carried out at from −20° C. to 180° C., preferably from 20° C. to 120° C., in an inert organic solvent in the presence of a base [cf. Houben-Weyl, Vol. 8 (1952), p. 560-589 and 610-612; Org. Reactions 8 (1954), 59 and 266]. In the formula IVb, X is a customary leaving group, such as halogen, alkoxy or alkylcarbonyloxy.

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, such as methylene chloride, chloroform and chlorobenzene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane and tetrahydrofuran, nitriles, and also dimethyl sulfoxide, dimethyl formamide and dimethyl acetamide, particularly preferably dimethylformamide, tetrahydrofuran, dimethyl sulfoxide, diethyl ether and toluene. It is also possible to employ mixtures of the abovementioned solvents.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal amides, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls, alkylmagnesium halides, and also alkali metal and alkaline earth metal alkoxides and dimethoxymagnesium, furthermore organic bases, for example tertiary amines, pyridine, substituted pyridines and also bicyclic amines. Particular preference is given to sodium hydride, sodium bicarbonate, sodium carbonate and sodium hydroxide and potassium hydroxide.

The bases are generally employed in equimolar amounts or in excess, but they can also be employed in catalytic amounts or, if appropriate, as solvent.

Suitable acylating agents are, for example, carbonyl halides, carboxylic anhydrides, chloroformates or carboxylic esters.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of acylating agent, based on IIIJ1#.

Compounds IIIJ# in which R^(B) is alkyl, haloalkyl, cycloalkyl, alkenyl, haloalkenyl, alkynyl or haloalkynyl are obtained by reacting the dicarbonyl compounds IIIJ2# with alkylhydrazines IVc. If the group L# is the phenoxy group E, the compounds IIIJ# correspond to the compounds IJ.

8) This reaction with alkylhydrazines is generally carried out at from −20° C. to 200° C., preferably from 20° C. to 150° C., in an inert organic solvent [cf. Org. Synthesis 55 (1976), 73; J. Am. Chem. Soc. 112 (1990), 7305; J. Org. Chem. 47 (1982), 214].

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, halogenated hydrocarbons, ethers, nitriles, alcohols, such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert-butanol, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide, particularly preferably methanol, ethanol or dimethylformamide. It is also posisble to employ mixtures of the abovementioned solvents.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of the alkylhydrazines, based on IIIJ2#.

The compounds IIIJ# in which R^(B) is hydrogen are obtained by reacting the dicarbonyl compounds IIIJ2# with hydrazine.

9) This reaction can be carried out similarly to the conditions described in Section 8) above.

Compounds IIIJ# in which R^(B) is alkyl, haloalkyl, cycloalkyl, alkenyl, haloalkenyl, alkynyl or haloalkynyl can alternatively also be obtained from the compounds IIIJ# in which R^(B) is hydrogen by alkylation. If the group L# is the phenoxy group E, the compounds IIIJ# correspond to the compounds IJ.

10) The alkylation of the diazolidinones IIIJ# is generally carried out at from −20° C. to 180° C., preferably from 20° C. to 120° C., in an inert organic solvent in the presence of a base [cf. Synth. Commun. 18 (1988), 2011; J. Chem. Soc. Chem. Commun., (1987), 735].

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisole and tetrahydrofuran, nitriles, alcohols, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide, particularly preferably dimethylformamide, tetrahydrofuran, dimethyl sulfoxide, diethyl ether and toluene. It is also possible to employ mixtures of the abovementioned solvents.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal amides, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls, alkylmagnesium halides, and also alkali metal and alkaline earth metal alkoxides and dimethoxymagnesium, furthermore organic bases, for example tertiary amines, pyridine, substituted pyridines and also bicyclic amines. Particular preference is given to sodium hydride, sodium bicarbonate, sodium carbonate and sodium hydroxide and potassium hydroxide.

The bases are generally employed in equimolar amounts or in excess, but they can also be employed in catalytic amounts or, if appropriate, as solvent.

Suitable alkylating agents are, for example, alkyl halides, alkyl sulfonates, alkyl p-toluenesulfonates, alkyl trifluoromethane-sulfonates, alcohols, ethers or alkyl p-bromophenylsulfonates, in particular methyl iodide or dimethyl sulfate.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of alkylating agent, based on IIIJ#.

Alternatively to the access route from the phenylacetic acid derivatives of the formula IIIG4#, the compounds IIIJ# can also be synthesized from carboxylic acid derivatives of the formula IIIJ3#. In the formula IIIJ3#, X is a leaving group, such as halogen or imidazolyl.

The reactions of IIIJ3# with hydrazine to give the compounds IIIJ# (R^(B)═H) and alkylation with alkylating agents [Alk] to give the compounds IIIJ#, or with alkylhydrazines IVc directly to give the compounds IIIJ#, are carried out by the methods of the reactions described in sections 9) to 11).

The compounds IIIJ3# are known from the literature [cf. WO-A 96/36229], or they can be prepared by the methods of the cited literature.

Alternatively, the dicarbonyl compounds IIIJ2# can also be prepared from aryl halides of the formula IIIJ4# by reaction with β-keto esters IVd under transition metal catalysis and subsequent alkylation.

11) This reaction is generally carried out at from −20° C. to 200° C., preferably from 20° C. to 150° C., in an inert organic solvent in the presence of a base and a catalyt [cf. Angew. Chem. Int. Ed. Engl. 13 (1974), 340; J. Am. Chem. Soc. 102 (1980), 7765; J. Am. Chem. Soc. 81 (1959), 627; Chem. Lett. 1981, 367].

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, ethers, ketones, and also dimethyl sulfoxide, dimethyl formamide and dimethylacetamide, particularly preferably dimethylformamide, toluene or xylene. It is also possible to use mixtures of the abovementioned solvents.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, alkali metal and alkaline earth metal oxides, alkali metal and alkaline earth metal hydrides, such as lithium hydride, sodium hydride, potassium hydride and calcium hydride, alkali metal amides, alkali metal and alkaline earth metal carbonates, and also alkali metal bicarbonates, organometallic compounds, in particular alkali metal alkyls, alkylmagnesium halides, and also alkali metal and alkaline earth metal alkoxides, furthermore organic bases, for example tertiary amines, pyridine, substituted pyridines and bicyclic amines. Particular preference is given to sodium hydride. The bases are generally employed in catalytic amounts, but they can also be employed in equimolar amounts, in excess or, if appropriate, as solvent.

Suitable catalysts are transition metals, such as, for example, copper, or their salts, in particular the halides, such as CuBr or CuCl.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of β-keto ester IVd, based on IIIJ4#.

12) The alkylation of IIIJ5# is carried out by the method of the reaction described in Section 6).

Compounds of the formulae IJ and IIIJ in which R^(C) is hydrogen are obtainable by reacting phenylacetic acid derivatives IIIG4# according to the acylation described in Section 7) directly to form compounds of the formula IIIJ2#, and carrying out the other steps analogously.

Alternatively, the radical R^(C) can also be introduced at the stage of the phenyldiazolidinone of the formula IIIJ#. If the group L# is the phenoxy group E, the compounds IIIJ# correspond to the compounds IJ.

13) This reaction is carried out similarly to the reaction described in Section 6).

The benzyl compounds IIIJ# required for preparing the compounds IJ in which R^(B) is hydroxyl, alkoxy, haloalkoxy, cycloalkyloxy, halocycloalkoxy, alkenyloxy, haloalkenyloxy, alkynyloxy, haloalkynyloxy or acetyloxy are obtainable by the following synthesis route:

14) This acylation with chloroformic esters is carried out similarly to the reaction described in Section 6).

Phenylmalonic esters IIIJ6# can alternatively be prepared from aryl halides of the formula IIIJ4# by reaction with malonic esters IVe under transition metal catalysis.

15) This reaction is carried out under the conditions described in Section 11).

The reaction of the phenylmalonic esters IIIJ6# with alkylhydrazines of the formula IVc leads to phenyldiazolidinediones of the formula IIIJ7#.

16) This reaction is carried out under the conditions described in Section 8).

The reaction of the phenylmalonic esters IIIJ6# with hydrazine likewise leads to phenyldiazolidinediones of the formula IIIJ7′#.

17) This reaction is carried out under the conditions described in Section 9).

Alkylations of the phenyldiazolidinediones IIIJ7# and IIIJ7′# lead to the compounds IIIJ′# and IIIJ7″#.

In the formula IIIJ′#, R′ is alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, alkynyl or haloalkynyl.

18) The alkylation is generally carried out at from 0° C. to 150° C., preferably from 20° C. to 100° C., in an inert organic solvent, if appropriate in the presence of a base [Arch. Pharm. 298 (1965), 580 ff.].

Suitable solvents are aliphatic hydrocarbons, aromatic hydrocarbons, halogenated hydrocarbons, such as methylene chloride, chloroform and chlorobenzene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane and tetrahydrofuran, nitriles, ketones, alcohols, and also dimethyl sulfoxide, dimethylformamide and dimethylacetamide, particularly preferably dimethylformamide, methylene chloride or tetrahydrofuran. It is also possible to employ mixtures of the abovementioned solvents.

Suitable bases are, in general, inorganic compounds, such as alkali metal and alkaline earth metal hydroxides, such as lithium hydroxide, sodium hydroxide, potassium hydroxide and calcium hydroxide, alkali metal and alkaline earth metal oxides, alkali metal and alkaline earth metal hydrides, alkali metal amides, alkali metal and alkaline earth metal carbonates, such as lithium carbonate, potassium carbonate and calcium carbonate, and also alkali metal bicarbonates, such as sodium bicarbonate, organometallic compounds, in particular alkali metal alkyls, alkylmagnesium halides, and also alkali metal and alkaline earth metal alkoxides and dimethoxymagnesium, furthermore organic bases, for example tertiary amines, such as trimethylamine, triethylamine, diisopropylethylamine and N-methylpiperidine, pyridine, substituted pyridines, and also bicyclic amines. Particular preference is given to potassium hydroxide, sodium hydroxide, potassium carbonate, triethylamine or pyridine. The bases are generally employed in equimolar amounts, in excess or, if appropriate, as solvent.

Suitable alkylating agents are, for example, diazoalkane compounds, alkyl halides, alkyl sulfonates, alkyl p-toluenesulfonates, alkyl trifluoromethanesulfonates, alcohols, ethers or alkyl p-bromophenylsulphonates, in particular methyl iodide, dimethyl sulfate or trimethylsilyldiazomethane.

The starting materials are generally reacted with each other in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of alkylating agent, based on IIIJ7#.

In the formula IIIJ″#, R′ is alkyl, haloalkyl, cycloalkyl, halocycloalkyl, alkenyl, haloalkenyl, alkynyl or haloalkynyl.

19) The alkylation is carried out similarly to the reaction described in Section 18) above.

The phenols of the formula II are known from the literature, and/or can be prepared similar to known methods [cf. EP-A 811 614; J. Org. Chem., Vol. 59 (1994) p. 1589; Bull. Chem. Soc. Jpn., Vol. 62 (1989) p. 618; J. Heterocycl. Chem., Vol. 27 (1990) p. 343; Chem. Lett. 1983, p. 1355; J. Heterocycl. Chem., Vol. 25 (1988) p. 1003; Tetrahedron Lett.; Vol. 29 (1988) p. 1425; Tetrahedron Lett., Vol. 27 (1986) p. 4407; Khim. Geterotsikl. Soedin 1991, p. 334; J. Chem. Soc., Perkin Trans., Vol. I 1990, p. 3112; Khim. Geterotsikl. Soedin (1968) p. 372; Chem. Ber., Vol. 94 (1961) p. 1868; J. Chem. Soc. (1952) p. 3418; J. Org. Chem., Vol. 53 (1988) p. 4349; Synth. Comm., Vol. 20 (1990) p. 3161; Chem. Lett. (1985) p. 1049; Synth. Comm., Vol. 20 (1990) p. 3161; Chem. Ber., Vol. 117 (1984) p. 1194].

The syntheses of the phenols II start either from phenols IIa or from phenyl compounds where a hydroxyl group can be generated from a suitable substituent Z. During the synthesis of the hetaryl group X, it may be necessary to block the hydroxyl function of the phenol derivative employed by a suitable protective group.

A suitable substituent Z may be, for example, a nitro group, which can be converted into a hydroxyl function by generally known methods via the reaction sequence: reduction, diazotization, reduction and boildown.

In the synthesis schemes below, [OH] denotes a hydroxyl group, which may be protected, or a suitable precursor thereof.

Phenols of the formula II in which X is pyrazol-1-yl are preferably obtained by the following method:

20a) The reaction of IIa with nitrite is carried out at −10° C. to 25° C., preferably at −5° C. to 10° C., in water or an inert organic solvent in the presence of an acid under generally customary conditions [cf. Organikum, 15th edition 1976, p. 654ff., VEB Verlag der Wissenschaften, Berlin].

The acids are generally used in equimolar amounts, in excess or, if appropriate, as solvents.

Nitrosating agents which are usually used are alkali metal or alkaline earth metal nitrites, in particular sodium nitrite or potassium nitrite.

The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of nitrosating agent, based on IIa.

20b) The reduction of the diazo compound can be carried out under generally customary conditions, preferably by reduction with iron, tin or zinc or salts thereof in the presence of an acid or by reduction with alkali metals in the presence of a base [cf. Houben-Weyl, Vol. IV/1c, 4th edition, p. 506ff., Thieme Verlag Stuttgart and New York (1980); ibid. Vol. IV/1d, 4th edition, p. 473ff. (1981); Heterocycles, Vol. 31, p. 2201 (1990)]. Preference is furthermore given to reducing the diazonium salts with sulfite or disulfite [cf: Organikum, 15th ed., VEB Verlag der Wissenschaften, Berlin, p. 662, 1976; J. Chem. Soc, 1927, p. 1325ff.; Chem. Ber., Vol. 55, p. 1827, 1922; Houben-Weyl, Vol. 10/2, p. 182, Thieme Verlag, Stuttgart].

The bases are generally employed in catalytic amounts, but it is also possible to employ them in equimolar amounts, in excess, or if appropriate, as solvents.

Suitable reducing agents are in particular NaHSO₃, Na₂S₂O₅ or SnCl₂.

The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of reducing agent, based on the nitroso compound.

21) The reaction of the hydrazine IIb with the β-keto compound IVf is usually carried out at −10° C. to 80° C., preferably at 0° C. to 30° C., in an inert organic solvent [cf. Synthesis (1991) p. 18; Heterocycles, Vol. 31 (1990) p. 855; J. Heterocycl. Chem., Vol. 24 (1987) p. 1309].

Suitable solvents are aliphatic hydrocarbons, such as pentane, hexane, cyclohexane and petroleum ether, aromatic hydrocarbons, such as toluene, o-, m- and p-xylene, halogenated hydrocarbons, such as methylene chloride, chloroform and chlorobenzene, ethers, such as diethyl ether, diisopropyl ether, tert-butyl methyl ether, dioxane, anisol and tetrahydrofuran, nitriles, such as acetonitrile and propionitrile, ketones such as acetone, methyl ethyl ketone, diethyl ketone and tert-butyl methyl ketone, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol and tert-butanol, and also dimethyl sulfoxide, dimethyl formamide and dimethylacetamide, particularly preferably methanol, ethanol or dimethylformamide. It is also possible to employ mixtures of the abovementioned solvents.

The starting materials are generally reacted with one another in equimolar amounts. In terms of yield, it may be advantageous to employ an excess of VIa, based on V#.

β-Ketocompounds IVf are either commercially available or they can be prepared by methods known from the literature.

Phenols of the formula II in which X is pyrazol-3-yl and pyrazol-5-yl, and also isoxazol-3-yl and isoxazol-5-yl, are preferably obtainable by the methods known from EP-A 811 614.

Phenols of the formula II in which X is 1,2,4-triazol-3-yl are obtainable by methods known from the literature, for example from the corresponding benzamides [cf. Liebigs Ann., Vol. 343 (1905) p. 207].

Phenols of the formula II in which Z is 1,3-oxazol-5-yl are obtainable by methods known from the literature from the corresponding α-aminoacetylbenzenes [cf. Chem. Ber., Vol. 47 (1914) p. 3163; J. Chem. Gen. USSR, Vol. 32 (1962) p. 1192].

Phenols of the formula II in which X is 1,3-oxazol-4-yl are obtainable by methods known from the literature from the corresponding α-haloacetylbenzenes [cf. Synth. Commun. (1979) p. 789].

Phenols of the formula II in which X is oxazol-2-yl are obtainable by routes known from the literature [cf. J. Chem. Soc., Perkin Trans., Vol. I (1990) p. 2329; Ind. J. Chem., Vol. 20 (1981) p. 322].

Phenols of the formula II in which X is imidazol-1-yl are obtainable by methods known from the literature [cf. J. Med. Chem., Vol. 31 (1988) p. 2136; J. Fluorine Chem., Vol. 43 (1989) p. 131; U.S. Pat No. 4,966,967].

Phenols of the formula II in which X is imidazol-2-yl are obtainable by routes known from the literature from phenyl halides and 2-trialkyltinimidazoles [cf. Bull. Chem. Soc. Jpn., Vol. 59 (1968) p. 677].

Phenols of the formula II in which X is imidazol-4-yl are obtainable by routes known from the literature from phenyl halides and 4-trialkyltinimidazoles [cf. Tetrahedron, Vol. 52 (1996) p. 13703].

Phenols of the formula II in which X is 1-alkylimidazol-5-yl are obtainable by routes known from the literature [cf. Tetrahedron Lett., Vol. 27 (1986) p. 5019].

Phenols of the formula II in which X is pyrrol-1-yl are obtainable, for example, by the following route known from the literature [cf. J. Heterocycl. Chem., Vol. 25 (1988) p. 1003; Tetrahedron Lett., Vol. 29 (1988) p. 1425]:

Phenols of the formula II in which X is pyrrol-2-yl are obtainable by methods known from the literature from aryl halides and pyrrol-2-yl Grignard compounds or the corresponding trimethyltin compounds [cf. Tetrahedron Lett., Vol. 27 (1986) p. 4407; Khim. Geterotsikl. Soedin (1991) p. 334; Tetrahedron Lett., Vol. 22 (1981) p. 5319].

The starting materials required for preparing the compounds I are known from the literature or can be prepared according to the literature cited.

If individual compounds I cannot be obtained by the routes described above, they can be prepared by derivatization of other compounds I.

The reaction mixtures are worked up in the customary manner, for example by mixing with water, phase separation and, if appropriate, chromatographic purification of the crude products. In some cases, the intermediates and end products are obtained in the form of colorless or pale brown viscous oils, which are purified or freed from volatile components under reduced pressure and at moderately elevated temperature. If the intermediates and end products are obtained as solids, they can also be purified by recrystallization or digestion.

Due to their C═C- and C═N-double bonds, the compounds I can be obtained from the preparation in the form of E/Z isomer mixtures, it being possible for these mixtures to be separated into the individual compounds in the customary manner, for example by crystallization or chromatography.

However, if the synthesis yields isomer mixtures, separation is generally not absolutely necessary since in some cases the individual isomers can be converted into each other during formulation for use or upon use (for example when exposed to light, acids or bases). Similar conversions can also take place after use, for example in the case of the treatment of plants in the treated plants or in the harmful fungus or the animal pest to be controlled.

In the definitions of the symbols given in the above formulae, collective terms were used which generally represent the following substituents:

Halogen: fluorine, chlorine, bromine and iodine;

Alkyl: saturated, straight-chain or branched hydrocarbon radicals having 1 to 4 carbon atoms, such as methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl or 1,1-dimethylethyl;

Haloalkyl: straight-chain or branched alkyl groups having 1 to 4 carbon atoms (as mentioned above), it being possible for the hydrogen atoms in these groups to be partially or fully replaced by halogen atoms as mentioned above, for example C₁-C₂-haloalkyl such as chloromethyl, bromomethyl, dichloromethyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, chlorofluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, 1-bromoethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 2-chloro-2-fluoroethyl, 2-chloro-2,2-difluoroethyl, 2,2-dichloro-2-fluoroethyl, 2,2,2-trichloroethyl and pentafluoroethyl;

Alkoxy: straight-chain or branched alkyl groups having 1 to 4 carbon atoms (as mentioned above), which are bonded to the skeleton via an oxygen atom (—O—);

Alkenyl: unsaturated, straight-chain or branched hydrocarbon radicals having 2 to 6 carbon atoms and a double bond in any position, such as ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl and 1-ethyl-2-methyl-2-propenyl;

Haloalkenyl: unsaturated, straight-chain or branched hydrocarbon radicals having 2 to 6 carbon atoms and a double bond in any position (as mentioned above), it being possible for the hydrogen atoms in these groups to be partially or fully replaced by halogen atoms as mentioned above, for example fluorine, chlorine and bromine;

Alkynyl: straight-chain or branched hydrocarbon groups having 2 to 6 carbon atoms and a triple bond in any position, such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl, 3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl, 1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl and 1-ethyl-1-methyl-2-propynyl;

Aryl: a mono- to trinuclear aromatic ring system containing 6 to 14 carbon ring members, for example phenyl, naphthyl and anthracenyl;

Five-membered hetaryl, containing one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom: 5-membered hetaryl groups which, in addition to carbon atoms, may contain one to four nitrogen atoms or one to three nitrogen atoms and one sulfur or oxygen atom as ring members, for example 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 1-pyrazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 1-imidazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 1,2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl, 1,2,4-thiadiazol- 3-yl, 1,2,4-thiadiazol-5-yl, 1,2,4-triazol-3-yl, 1,3,4-oxadiazol- 2-yl, 1,3,4-thiadiazol-2-yl and 1,3,4-triazol-2-yl;

Alkylene: divalent unbranched chains of 3 to 5 CH₂ groups, for example CH₂, CH₂CH₂, CH₂CH₂CH₂, CH₂CH₂CH₂CH₂ and CH₂CH₂CH₂CH₂CH₂.

Customary groups are in particular the following substituents: halogen, cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylamino, di-C₁-C₄-alkylamino and C₁-C₄-alkylthio.

With regard to the variables, the particularly preferred embodiments of the intermediates correspond to those of the radicals Q, X, Y_(n), Y¹ _(m) and Y² _(p) of the formula I.

With a view to the intended use of the phenyl compounds of the formula I, particular preference is given to the following meanings of the substituents, in each case either alone or in combination:

Preference is given to compounds I′.

Particular preference is given to compounds I in which Q is C(═CHOCH₃)—COOCH₃, C(═CHCH₃)—COOCH₃, C(═NOCH₃)—COOCH₃, C(═NOCH₃)—CONHCH₃ or N(—OCH₃)—COOCH₃.

In addition, preference is given to compounds I in which Y¹ is ortho to the oxymethylene group.

Likewise, preference is given to compounds I in which Y_(n) is 6-methyl.

Furthermore, preference is given to compounds I in which the index m is 1 or 2.

Additionally, preference is also given to compounds I″.

Particular preference is given to compounds I in which X is pyrazol-1-yl.

Particular preference is also given to compounds IA in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl, X is pyrazol-1-yl, pyrazol-3-yl, pyrazol-5-yl, isoxazol-3-yl, isoxazol-5-yl, 1,2,4-triazol-3-yl, oxazol-2-yl, oxazol-4-yl or oxazol-5-yl, in each case substituted by customary groups.

Likewise, particular preference is given to compounds IB in which R^(A) is hydrogen, chlorine, methyl or methoxy, Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl, X is pyrazol-1-yl, pyrazol-3-yl, pyrazol-5-yl, isoxazol-3-yl, isoxazol-5-yl, 1,2,4-triazol-3-yl, oxazol-2-yl, oxazol-4-yl or oxazol-5-yl, in each case substituted by customary groups.

Additionally, particular preference is given to compounds IC in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl, X is pyrazol-1-yl, pyrazol-3-yl, pyrazol-5-yl, isoxazol-3-yl, isoxazol-5-yl, 1,2,4-triazol-3-yl, oxazol-2-yl, oxazol-4-yl or oxazol-5-yl, each of which is substituted by customary groups.

Particular preference is also given to compounds ID in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl, R^(C) is hydrogen or methyl, X is pyrazol-1-yl, pyrazol-3-yl, pyrazol-5-yl, isoxazol-3-yl, isoxazol-5-yl, 1,2,4-triazol-3-yl, oxazol-2-yl, oxazol-4-yl or oxazol-5-yl, in each case substituted by customary groups.

Furthermore, particular preference is given to compounds IE, in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl, X is pyrazol-1-yl, pyrazol-3-yl, pyrazol-5-yl, isoxazol-3-yl, isoxazol-5-yl, 1,2,4-triazol-3-yl, oxazol-2-yl, oxazol-4-yl or oxazol-5-yl, in each case substituted by customary groups.

Moreover, particular preference is given to compounds IF″ in which R^(A) is chlorine, methyl or methoxy, Y¹ is chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl, X is pyrazol-1-yl, pyrazol-3-yl, pyrazol-5-yl, isoxazol-3-yl, isoxazol-5-yl, 1,2,4-triazol-3-yl, oxazol-2-yl, oxazol-4-yl or oxazol-5-yl, in each case substituted by customary groups.

Likewise, particular preference is given to compounds IG″ in which R^(A) is chlorine, methyl or methoxy, Y¹ is chlorine or methyl, Y1′ is hydrogen, chlorine or methyl, X is pyrazol-1-yl, pyrazol-3-yl, pyrazol-5-yl, isoxazol-3-yl, isoxazol-5-yl, 1,2,4-triazol-3-yl, oxazol-2-yl, oxazol-4-yl or oxazol-5-yl, in each case substituted by customary groups.

Additionally, particular preference is given to compounds 1H″ in which Y¹ is chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl, X is pyrazol-1-yl, pyrazol-3-yl, pyrazol-5-yl, isoxazol-3-yl, isoxazol-5-yl, 1,2,4-triazol-3-yl, oxazol-2-yl, oxazol-4-yl or oxazol-5-yl, in each case substituted by customary groups.

Particular preference is also given to compounds IJ″ in which R^(A) is chlorine, methyl or methoxy, Y¹ is chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl, R^(C) is hydrogen or methyl, X is pyrazol-1-yl, pyrazol-3-yl, pyrazol-5-yl, isoxazol-3-yl, isoxazol-5-yl, 1,2,4-triazol-3-yl, oxazol-2-yl, oxazol-4-yl or oxazol-5-yl, in each case substituted by customary groups.

Additionally, particular preference is given to compounds I.1 in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl, and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Likewise, particular preference is given to compounds I.2, in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Additionally, particular preference is given to compounds I.3 in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Furthermore, particular preference is given to compounds I.4 in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Additionally, particular preference is given to compounds I.5 in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Likewise, particular preference is given to compounds I.6, in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Additionally, particular preference is given to compounds I.7 in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Likewise, particular preference is given to compounds I.8, in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Additionally, particular preference is given to compounds I.9 in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Particular preference is also given to compounds I.10 in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Additionally, particular preference is given to compounds I.11 in which Y¹ is hydrogen, chlorine or methyl, Y¹ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Likewise, particular preference is given to compounds I.12, in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

Additionally, particular preference is given to compounds I.13 in which Y¹ is hydrogen, chlorine or methyl, Y¹′ is hydrogen, chlorine or methyl and R¹, R² and R³ are hydrogen, halogen, C₁-C₄-alkyl or trifluoromethyl.

With respect to their use, the compounds I compiled in the tables below are particularly preferred. In addition, the groups mentioned for a substituent in the tables represent themselves, independently of the combination in which they are mentioned, a particularly preferred embodiment of the substituent in question.

Table 1

Compounds of the formula IA.1 in which Y¹ is chlorine, Y¹′ represents hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 2

Compounds of the formula IA.1 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 3

Compounds of the formula IA.1 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 4

Compounds of the formula IA.1 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 5

Compounds of the formula IA.1 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 6

Compounds of the formula IA.1 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 7

Compounds of the formula IA.1 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 8

Compounds of the formula IA.1 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 9

Compounds of the formula IA.1 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 10

Compounds of the formula IA.2 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 11

Compounds of the formula IA.2 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 12

Compounds of the formula IA.2 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 13

Compounds of the formula IA.2 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 14

Compounds of the formula IA.2 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 15

Compounds of the formula IA.2 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 16

Compounds of the formula IA.2 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 17

Compounds of the formula IA.2 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 18

Compounds of the formula IA.2 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 19

Compounds of the formula IA.3 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 20

Compounds of the formula IA.3 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 21

Compounds of the formula IA.3 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 22

Compounds of the formula IA.3 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 23

Compounds of the formula IA.3 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 24

Compounds of the formula IA.3 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 25

Compounds of the formula IA.3 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 26

Compounds of the formula IA.3 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 27

Compounds of the formula IA.3 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 28

Compounds of the formula IA.4 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 29

Compounds of the formula IA.4 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 30

Compounds of the formula IA.4 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 31

Compounds of the formula IA.4 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 32

Compounds of the formula IA.4 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 33

Compounds of the formula IA.4 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 34

Compounds of the formula IA.4 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 35

Compounds of the formula IA.4 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 36

Compounds of the formula IA.4 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 37

Compounds of the formula IA.5 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 38

Compounds of the formula IA.5 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 39

Compounds of the formula IA.5 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 40

Compounds of the formula IA.5 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 41

Compounds of the formula IA.5 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 42

Compounds of the formula IA.5 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 43

Compounds of the formula IA.5 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 44

Compounds of the formula IA.5 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 45

Compounds of the formula IA.5 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 46

Compounds of the formula IA.6 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 47

Compounds of the formula IA.6 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 48

Compounds of the formula IA.6 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 49

Compounds of the formula IA.6 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 50

Compounds of the formula IA.6 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 51

Compounds of the formula IA.6 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 52

Compounds of the formula IA.6 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 53

Compounds of the formula IA.6 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 54

Compounds of the formula IA.6 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 55

Compounds of the formula IA.7 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 56

Compounds of the formula IA.7 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 57

Compounds of the formula IA.7 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 58

Compounds of the formula IA.7 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 59

Compounds of the formula IA.7 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 60

Compounds of the formula IA.7 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 61

Compounds of the formula IA.7 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 62

Compounds of the formula IA.7 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 63

Compounds of the formula IA.7 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 64

Compounds of the formula IA.8 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 65

Compounds of the formula IA.8 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 66

Compounds of the formula IA.8 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 67

Compounds of the formula IA.8 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 68

Compounds of the formula IA.8 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 69

Compounds of the formula IA.8 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 70

Compounds of the formula IA.8 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 71

Compounds of the formula IA.8 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 72

Compounds of the formula IA.8 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 73

Compounds of the formula IA.9 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 74

Compounds of the formula IA.9 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 75

Compounds of the formula IA.9 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 76

Compounds of the formula IA.9 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 77

Compounds of the formula IA.9 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 78

Compounds of the formula IA.9 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 79

Compounds of the formula IA.9 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 80

Compounds of the formula IA.9 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 81

Compounds of the formula IA.9 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 82

Compounds of the formula IA.10 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 83

Compounds of the formula IA.10 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 84

Compounds of the formula IA.10 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 85

Compounds of the formula IA.10 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 86

Compounds of the formula IA.10 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 87

Compounds of the formula IA.10 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 88

Compounds of the formula IA.10 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 89

Compounds of the formula IA.10 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 90

Compounds of the formula IA.10 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 91

Compounds of the formula IA.ll in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 92

Compounds of the formula IA.11 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 93

Compounds of the formula IA.11 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 94

Compounds of the formula IA.11 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 95

Compounds of the formula IA.11 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 96

Compounds of the formula IA.11 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 97

Compounds of the formula IA.11 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 98

Compounds of the formula IA.11 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 99

Compounds of the formula IA.11 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 100

Compounds of the formula IA.12 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 101

Compounds of the formula IA.12 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 102

Compounds of the formula IA.12 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 103

Compounds of the formula IA.12 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 104

Compounds of the formula IA.12 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 105

Compounds of the formula IA.12 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 106

Compounds of the formula IA.12 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 107

Compounds of the formula IA.12 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 108

Compounds of the formula IA.12 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 109

Compounds of the formula IA.13 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 110

Compounds of the formula IA.13 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 111

Compounds of the formula IA.13 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 112

Compounds of the formula IA.13 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 113

Compounds of the formula IA.13 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 114

Compounds of the formula IA.13 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 115

Compounds of the formula IA.13 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 116

Compounds of the formula IA.13 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 117

Compounds of the formula IA.13 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 118

Compounds of the formula IB.1 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 119

Compounds of the formula IB.1 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 120

Compounds of the formula IB.1 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 121

Compounds of the formula IB.1 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 122

Compounds of the formula IB.1 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 123

Compounds of the formula IB.1 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 124

Compounds of the formula IB.1 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 125

Compounds of the formula IB.1 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 126

Compounds of the formula IB.1 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 127

Compounds of the formula IB.2 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 128

Compounds of the formula IB.2 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 129

Compounds of the formula IB.2 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 130

Compounds of the formula IB.2 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 131

Compounds of the formula IB.2 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 132

Compounds of the formula IB.2 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 133

Compounds of the formula IB.2 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 134

Compounds of the formula IB.2 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 135

Compounds of the formula IB.2 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 136

Compounds of the formula IB.3 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 137

Compounds of the formula IB.3 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 138

Compounds of the formula IB.3 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 139

Compounds of the formula IB.3 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 140

Compounds of the formula IB.3 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 141

Compounds of the formula IB.3 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 142

Compounds of the formula IB.3 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 143

Compounds of the formula IB.3 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 144

Compounds of the formula IB.3 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 145

Compounds of the formula IB.4 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 146

Compounds of the formula IB.4 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 147

Compounds of the formula IB.4 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 148

Compounds of the formula IB.4 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 149

Compounds of the formula IB.4 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 150

Compounds of the formula IB.4 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 151

Compounds of the formula IB.4 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 152

Compounds of the formula IB.4 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 153

Compounds of the formula IB.4 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 154

Compounds of the formula IB.5 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 155

Compounds of the formula IB.5 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 156

Compounds of the formula IB.5 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 157

Compounds of the formula IB.5 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 158

Compounds of the formula IB.5 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 159

Compounds of the formula IB.5 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 160

Compounds of the formula IB.5 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 161

Compounds of the formula IB.5 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 162

Compounds of the formula IB.5 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 163

Compounds of the formula IB.6 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 164

Compounds of the formula IB.6 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 165

Compounds of the formula IB.6 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 166

Compounds of the formula IB.6 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 167

Compounds of the formula IB.6 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 168

Compounds of the formula IB.6 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 169

Compounds of the formula IB.6 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 170

Compounds of the formula IB.6 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 171

Compounds of the formula IB.6 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 172

Compounds of the formula IB.7 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 173

Compounds of the formula IB.7 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 174

Compounds of the formula IB.7 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 175

Compounds of the formula IB.7 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 176

Compounds of the formula IB.7 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 177

Compounds of the formula IB.7 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 178

Compounds of the formula IB.7 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 179

Compounds of the formula IB.7 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 180

Compounds of the formula IB.7 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 181

Compounds of the formula IB.8 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 182

Compounds of the formula IB.8 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 183

Compounds of the formula IB.8 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 184

Compounds of the formula IB.8 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 185

Compounds of the formula IB.8 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 186

Compounds of the formula IB.8 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 187

Compounds of the formula IB.8 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 188

Compounds of the formula IB.8 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 189

Compounds of the formula IB.8 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 190

Compounds of the formula IB.9 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 191

Compounds of the formula IB.9 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 192

Compounds of the formula IB.9 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 193

Compounds of the formula IB.9 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 194

Compounds of the formula IB.9 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 195

Compounds of the formula IB.9 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 196

Compounds of the formula IB.9 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 197

Compounds of the formula IB.9 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 198

Compounds of the formula IB.9 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 199

Compounds of the formula IB.10 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 200

Compounds of the formula IB.10 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 201

Compounds of the formula IB.10 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 202

Compounds of the formula IB.10 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals Rim R² and R³ corresponds for each compound to one row of Table D

Table 203

Compounds of the formula IB.l0 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 204

Compounds of the formula IB.10 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 205

Compounds of the formula IB.10 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 206

Compounds of the formula IB.10 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 207

Compounds of the formula IB.10 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 208

Compounds of the formula IB.11 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 209

Compounds of the formula IB.11 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 210

Compounds of the formula IB.11 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 211

Compounds of the formula IB.11 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 212

Compounds of the formula IB.11 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 213

Compounds of the formula IB.11 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 214

Compounds of the formula IB.11 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 215

Compounds of the formula IB.11 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 216

Compounds of the formula IB.11 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 217

Compounds of the formula IB.12 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 218

Compounds of the formula IB.12 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 219

Compounds of the formula IB.12 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 220

Compounds of the formula IB.12 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 221

Compounds of the formula IB.12 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 222

Compounds of the formula IB.12 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 223

Compounds of the formula IB.12 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 224

Compounds of the formula IB.12 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 225

Compounds of the formula IB.12 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 226

Compounds of the formula IB.13 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 227

Compounds of the formula IB.13 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 228

Compounds of the formula IB.13 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 229

Compounds of the formula IB.13 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 230

Compounds of the formula IB.13 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 231

Compounds of the formula IB.13 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 232

Compounds of the formula IB.13 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 233

Compounds of the formula IB.13 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 234

Compounds of the formula IB.13 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 235

Compounds of the formula IC.1 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 236

Compounds of the formula IC.1 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 237

Compounds of the formula IC.1 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 238

Compounds of the formula IC.1 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 239

Compounds of the formula IC.1 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 240

Compounds of the formula IC.1 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 241

Compounds of the formula IC.1 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 242

Compounds of the formula IC.1 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals Rib R² and R³ corresponds for each compound to one row of Table A

Table 243

Compounds of the formula IC.1 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 244

Compounds of the formula IC.2 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 245

Compounds of the formula IC.2 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 246

Compounds of the formula IC.2 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 247

Compounds of the formula IC.2 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 248

Compounds of the formula IC.2 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 249

Compounds of the formula IC.2 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ ₁ R² and R³ corresponds for each compound to one row of Table A

Table 250

Compounds of the formula IC.2 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 251

Compounds of the formula IC.2 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 252

Compounds of the formula IC.2 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 253

Compounds of the formula IC.3 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 254

Compounds of the formula IC.3 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 255

Compounds of the formula IC.3 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 256

Compounds of the formula IC.3 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 257

Compounds of the formula IC.3 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 258

Compounds of the formula IC.3 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 259

Compounds of the formula IC.3 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 260

Compounds of the formula IC.3 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 261

Compounds of the formula IC.3 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 262

Compounds of the formula IC.4 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 263

Compounds of the formula IC.4 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 264

Compounds of the formula IC.4 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 265

Compounds of the formula IC.4 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 266

Compounds of the formula IC.4 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 267

Compounds of the formula IC.4 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 268

Compounds of the formula IC.4 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 269

Compounds of the formula IC.4 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 270

Compounds of the formula IC.4 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 271

Compounds of the formula IC.5 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 272

Compounds of the formula IC.5 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 273

Compounds of the formula IC.5 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 274

Compounds of the formula IC.5 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds or each compound to one row of Table B

Table 275

Compounds of the formula IC.5 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 276

Compounds of the formula IC.5 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 277

Compounds of the formula IC.5 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 278

Compounds of the formula IC.5 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 279

Compounds of the formula IC.5 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 280

Compounds of the formula IC.6 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 281

Compounds of the formula IC.6 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 282

Compounds of the formula IC.6 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 283

Compounds of the formula IC.6 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 284

Compounds of the formula IC.6 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 285

Compounds of the formula IC.6 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compouand to one row of Table C

Table 286

Compounds of the formula IC.6 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 287

Compounds of the formula IC.6 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 288

Compounds of the formula IC.6 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 289

Compounds of the formula IC.7 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 290

Compounds of the formula IC.7 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 291

Compounds of the formula IC.7 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 292

Compounds of the formula IC.7 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 293

Compounds of the formula IC.7 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 294

Compounds of the formula IC.7 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 295

Compounds of the formula IC.7 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 296

Compounds of the formula IC.7 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 297

Compounds of the formula IC.7 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 298

Compounds of the formula IC.8 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 299

Compounds of the formula IC.8 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 300

Compounds of the formula IC.8 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 301

Compounds of the formula IC.8 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 302

Compounds of the formula IC.8 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 303

Compounds of the formula IC.8 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 304

Compounds of the formula IC.8 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 305

Compounds of the formula IC.8 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 306

Compounds of the formula IC.8 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 307

Compounds of the formula IC.9 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 308

Compounds of the formula IC.9 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 309

Compounds of the formula IC.9 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 310

Compounds of the formula IC.9 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 311

Compounds of the formula IC.9 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 312

Compounds of the formula IC.9 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 313

Compounds of the formula IC.9 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 314

Compounds of the formula IC.9 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 315

Compounds of the formula IC.9 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 316

Compounds of the formula IC.10 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 317

Compounds of the formula IC.10 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 318

Compounds of the formula IC.10 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 319

Compounds of the formula IC.10 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 320

Compounds of the formula IC.10 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 321

Compounds of the formula IC.10 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 322

Compounds of the formula IC.10 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 323

Compounds of the formula IC.10 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 324

Compounds of the formula IC.10 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 325

Compounds of the formula IC.11 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 326

Compounds of the formula IC.11 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 327

Compounds of the formula IC.11 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 328

Compounds of the formula IC.11 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 329

Compounds of the formula IC.11 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 330

Compounds of the formula IC.11 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 331

Compounds of the formula IC.11 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 332

Compounds of the formula IC.11 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 333

Compounds of the formula IC.11 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 334

Compounds of the formula IC.12 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 335

Compounds of the formula IC.12 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 336

Compounds of the formula IC.12 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 337

Compounds of the formula IC.12 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 338

Compounds of the formula IC.12 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 339

Compounds of the formula IC.12 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 340

Compounds of the formula IC.12 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 341

Compounds of the formula IC.12 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 342

Compounds of the formula IC.12 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 343

Compounds of the formula IC.13 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 344

Compounds of the formula IC.13 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 345

Compounds of the formula IC.13 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 346

Compounds of the formula IC.13 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 347

Compounds of the formula IC.13 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 348

Compounds of the formula IC.13 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 349

Compounds of the formula IC.13 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 350

Compounds of the formula IC.13 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 351

Compounds of the formula IC.13 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 352

Compounds of the formula ID.1 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 353

Compounds of the formula ID.1 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 354

Compounds of the formula ID.1 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 355

Compounds of the formula ID.1 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 356

Compounds of the formula ID.1 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 357

Compounds of the formula ID.1 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 358

Compounds of the formula ID.1 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 359

Compounds of the formula ID.1 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 360

Compounds of the formula ID.1 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 361

Compounds of the formula ID.2 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 362

Compounds of the formula ID.2 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 363

Compounds of the formula ID.2 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 364

Compounds of the formula ID.2 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 365

Compounds of the formula ID.2 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 366

Compounds of the formula ID.2 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 367

Compounds of the formula ID.2 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 368

Compounds of the formula ID.2 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 369

Compounds of the formula ID.2 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 370

Compounds of the formula ID.3 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 371

Compounds of the formula ID.3 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 372

Compounds of the formula ID.3 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 373

Compounds of the formula ID.3 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 374

Compounds of the formula ID.3 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 375

Compounds of the formula ID.3 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 376

Compounds of the formula ID.3 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 377

Compounds of the formula ID.3 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 378

Compounds of the formula ID.3 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 379

Compounds of the formula ID.4 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 380

Compounds of the formula ID.4 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 381

Compounds of the formula ID.4 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 382

Compounds of the formula ID.4 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 383

Compounds of the formula ID.4 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 384

Compounds of the formula ID.4 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 385

Compounds of the formula ID.4 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 386

Compounds of the formula ID.4 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 387

Compounds of the formula ID.4 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 388

Compounds of the formula ID.5 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 389

Compounds of the formula ID.5 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 390

Compounds of the formula ID.5 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 391

Compounds of the formula ID.5 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 392

Compounds of the formula ID.5 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 393

Compounds of the formula ID.5 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 394

Compounds of the formula ID.5 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 395

Compounds of the formula ID.5 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 396

Compounds of the formula ID.5 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 397

Compounds of the formula ID.6 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 398

Compounds of the formula ID.6 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 399

Compounds of the formula ID.6 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 400

Compounds of the formula ID.6 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 401

Compounds of the formula ID.6 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 402

Compounds of the formula ID.6 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 403

Compounds of the formula ID.6 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 404

Compounds of the formula ID.6 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds or each compound to one row of Table C

Table 405

Compounds of the formula ID.6 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 406

Compounds of the formula ID.7 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 407

Compounds of the formula ID.7 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 408

Compounds of the formula ID.7 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 409

Compounds of the formula ID.7 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 410

Compounds of the formula ID.7 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 411

Compounds of the formula ID.7 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 412

Compounds of the formula ID.7 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 413

Compounds of the formula ID.7 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 414

Compounds of the formula ID.7 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 415

Compounds of the formula ID.8 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 416

Compounds of the formula ID.8 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 417

Compounds of the formula ID.8 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 418

Compounds of the formula ID.8 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 419

Compounds of the formula ID.8 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 420

Compounds of the formula ID.8 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to the one row of Table B

Table 421

Compounds of the formula ID.8 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 422

Compounds of the formula ID.8 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 423

Compounds of the formula ID.8 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 424

Compounds of the formula ID.9 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 425

Compounds of the formula ID.9 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 426

Compounds of the formula ID.9 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 427

Compounds of the formula ID.9 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 428

Compounds of the formula ID.9 in which Y¹ is methyl, Y^(1,) is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 429

Compounds of the formula ID.9 in which Y¹ is methyl, Y^(1,) is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 430

Compounds of the formula ID.9 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 431

Compounds of the formula ID.9 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 432

Compounds of the formula ID.9 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 433

Compounds of the formula ID.10 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 434

Compounds of the formula ID.10 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 435

Compounds of the formula ID.10 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 436

Compounds of the formula ID.10 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 437

Compounds of the formula ID.10 in which Y¹ is methyl, Y¹ ′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 438

Compounds of the formula ID.10 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 439

Compounds of the formula ID.10 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 440

Compounds of the formula ID.10 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 441

Compounds of the formula ID.10 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 442

Compounds of the formula ID.11 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 443

Compounds of the formula ID.11 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 444

Compounds of the formula ID.11 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 445

Compounds of the formula ID.11 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 446

Compounds of the formula ID.11 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 447

Compounds of the formula ID.11 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 448

Compounds of the formula ID.11 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 449

Compounds of the formula ID.11 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 450

Compounds of the formula ID.11 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 451

Compounds of the formula ID.12 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 452

Compounds of the formula ID.12 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 453

Compounds of the formula ID.12 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 454

Compounds of the formula ID.12 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 455

Compounds of the formula ID.12 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 456

Compounds of the formula ID.12 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 457

Compounds of the formula ID.12 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 458

Compounds of the formula ID.12 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 459

Compounds of the formula ID.12 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 460

Compounds of the formula ID.13 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 461

Compounds of the formula ID.13 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 462

Compounds of the formula ID.13 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 463

Compounds of the formula ID.13 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 464

Compounds of the formula ID.13 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 465

Compounds of the formula ID.13 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 466

Compounds of the formula ID.13 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 467

Compounds of the formula ID.13 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 468

Compounds of the formula ID.13 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 469

Compounds of the formula IE.1 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 470

Compounds of the formula IE.1 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 471

Compounds of the formula IE.1 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 472

Compounds of the formula IE.1 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 473

Compounds of the formula IE.1 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 474

Compounds of the formula IE.1 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 475

Compounds of the formula IE.1 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 476

Compounds of the formula IE.1 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 477

Compounds of the formula IE.1 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 478

Compounds of the formula IE.2 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 479

Compounds of the formula IE.2 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 480

Compounds of the formula IE.2 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 481

Compounds of the formula IE.2 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 482

Compounds of the formula IE.2 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 483

Compounds of the formula IE.2 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 484

Compounds of the formula IE.2 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 485

Compounds of the formula IE.2 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 486

Compounds of the formula IE.2 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 487

Compounds of the formula IE.3 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 488

Compounds of the formula IE.3 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 489

Compounds of the formula IE.3 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 490

Compounds of the formula IE.3 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 491

Compounds of the formula IE.3 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 492

Compounds of the formula IE.3 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 493

Compounds of the formula IE.3 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 494

Compounds of the formula IE.3 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 495

Compounds of the formula IE.3 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 496

Compounds of the formula IE.4 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 497

Compounds of the formula IE.4 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 498

Compounds of the formula IE.4 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 499

Compounds of the formula IE.4 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 500

Compounds of the formula IE.4 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 501

Compounds of the formula IE.4 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 502

Compounds of the formula IE.4 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 503

Compounds of the formula IE.4 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 504

Compounds of the formula IE.4 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 505

Compounds of the formula IE.5 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 506

Compounds of the formula IE.5 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 507

Compounds of the formula IE.5 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 508

Compounds of the formula IE.5 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 509

Compounds of the formula IE.5 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 510

Compounds of the formula IE.5 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 511

Compounds of the formula IE.5 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 512

Compounds of the formula IE.5 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 513

Compounds of the formula IE.5 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 514

Compounds of the formula IE.6 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 515

Compounds of the formula IE.6 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 516

Compounds of the formula IE.6 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 517

Compounds of the formula IE.6 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 518

Compounds of the formula IE.6 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 519

Compounds of the formula IE.6 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 520

Compounds of the formula IE.6 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 521

Compounds of the formula IE.6 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 522

Compounds of the formula IE.6 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 523

Compounds of the formula IE.7 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 524

Compounds of the formula IE.7 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 525

Compounds of the formula IE.7 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 526

Compounds of the formula IE.7 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 527

Compounds of the formula IE.7 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 528

Compounds of the formula IE.7 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 529

Compounds of the formula IE.7 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 530

Compounds of the formula IE.7 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 531

Compounds of the formula IE.7 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 532

Compounds of the formula IE.8 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 533

Compounds of the formula IE.8 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 534

Compounds of the formula IE.8 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 535

Compounds of the formula IE.8 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 536

Compounds of the formula IE.8 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 537

Compounds of the formula IE.8 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 538

Compounds of the formula IE.8 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 539

Compounds of the formula IE.8 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 540

Compounds of the formula IE.8 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 541

Compounds of the formula IE.9 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 542

Compounds of the formula IE.9 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 543

Compounds of the formula IE.9 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 544

Compounds of the formula IE.9 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 545

Compounds of the formula IE.9 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 546

Compounds of the formula IE.9 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 547

Compounds of the formula IE.9 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 548

Compounds of the formula IE.9 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 549

Compounds of the formula IE.9 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 550

Compounds of the formula IE.10 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 551

Compounds of the formula IE.10 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 552

Compounds of the formula IE.10 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 553

Compounds of the formula IE.10 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 554

Compounds of the formula IE.10 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 555

Compounds of the formula IE.10 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 556

Compounds of the formula IE.10 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 557

Compounds of the formula IE.10 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 558

Compounds of the formula IE.10 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 559

Compounds of the formula IE.11 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 560

Compounds of the formula IE.11 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 561

Compounds of the formula IE.11 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 562

Compounds of the formula IE.11 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 563

Compounds of the formula IE.11 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 564

Compounds of the formula IE.11 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 565

Compounds of the formula IE.11 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 566

Compounds of the formula IE.11 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 567

Compounds of the formula IE.11 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 568

Compounds of the formula IE.12 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 569

Compounds of the formula IE.12 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 570

Compounds of the formula IE.12 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 571

Compounds of the formula IE.12 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 572

Compounds of the formula IE.12 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 573

Compounds of the formula IE.12 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 574

Compounds of the formula IE.12 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 575

Compounds of the formula IE.12 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 576

Compounds of the formula IE.12 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 577

Compounds of the formula IE.13 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 578

Compounds of the formula IE.13 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 579

Compounds of the formula IE.13 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 580

Compounds of the formula IE.13 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 581

Compounds of the formula IE.13 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 582

Compounds of the formula IE.13 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 583

Compounds of the formula IE.13 in which Y¹ is hydrogen, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 584

Compounds of the formula IE.13 in which Y¹ is hydrogen, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 585

Compounds of the formula IE.13 in which Y¹ is hydrogen, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 586

Compounds of the formula IF.1 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 587

Compounds of the formula IF.1 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 588

Compounds of the formula IF.1 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 589

Compounds of the formula IF.1 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 590

Compounds of the formula IF.1 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 591

Compounds of the formula IF.1 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 592

Compounds of the formula IF.1 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 593

Compounds of the formula IF.1 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 594

Compounds of the formula IF.1 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 595

Compounds of the formula IF.1 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 596

Compounds of the formula IF.1 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 597

Compounds of the formula IF.1 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 598

Compounds of the formula IF.1 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 599

Compounds of the formula IF.1 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 600

Compounds of the formula IF.1 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 601

Compounds of the formula IF.1 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 602

Compounds of the formula IF.1 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 603

Compounds of the formula IF.1 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 604

Compounds of the formula IF.2 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 605

Compounds of the formula IF.2 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 606

Compounds of the formula IF.2 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 607

Compounds of the formula IF.2 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 608

Compounds of the formula IF.2 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 609

Compounds of the formula IF.2 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 610

Compounds of the formula IF.2 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 611

Compounds of the formula IF.2 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 612

Compounds of the formula IF.2 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 613

Compounds of the formula IF.2 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 614

Compounds of the formula IF.2 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 615

Compounds of the formula IF.2 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 616

Compounds of the formula IF.2 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 617

Compounds of the formula IF.2 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 618

Compounds of the formula IF.2 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 619

Compounds of the formula IF.2 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 620

Compounds of the formula IF.2 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 621

Compounds of the formula IF.2 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 622

Compounds of the formula IF.3 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 623

Compounds of the formula IF.3 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 624

Compounds of the formula IF.3 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 625

Compounds of the formula IF.3 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 626

Compounds of the formula IF.3 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 627

Compounds of the formula IF.3 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 628

Compounds of the formula IF.3 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 629

Compounds of the formula IF.3 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 630

Compounds of the formula IF.3 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 631

Compounds of the formula IF.3 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 632

Compounds of the formula IF.3 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 633

Compounds of the formula IF.3 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 634

Compounds of the formula IF.3 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 635

Compounds of the formula IF.3 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 636

Compounds of the formula IF.3 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 637

Compounds of the formula IF.3 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 638

Compounds of the formula IF.3 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 639

Compounds of the formula IF.3 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 640

Compounds of the formula IF.4 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 641

Compounds of the formula IF.4 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 642

Compounds of the formula IF.4 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 643

Compounds of the formula IF.4 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 644

Compounds of the formula IF.4 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 645

Compounds of the formula IF.4 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 646

Compounds of the formula IF.4 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 647

Compounds of the formula IF.4 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 648

Compounds of the formula IF.4 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 649

Compounds of the formula IF.4 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 650

Compounds of the formula IF.4 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 651

Compounds of the formula IF.4 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 652

Compounds of the formula IF.4 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 653

Compounds of the formula IF.4 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 654

Compounds of the formula IF.4 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 655

Compounds of the formula IF.4 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 656

Compounds of the formula IF.4 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 657

Compounds of the formula IF.4 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 658

Compounds of the formula IF.5 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 659

Compounds of the formula IF.5 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 660

Compounds of the formula IF.5 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 661

Compounds of the formula IF.5 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 662

Compounds of the formula IF.5 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 663

Compounds of the formula IF.5 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 664

Compounds of the formula IF.5 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 665

Compounds of the formula IF.5 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 666

Compounds of the formula IF.5 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 667

Compounds of the formula IF.5 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 668

Compounds of the formula IF.5 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 669

Compounds of the formula IF.5 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 670

Compounds of the formula IF.5 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 671

Compounds of the formula IF.5 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 672

Compounds of the formula IF.5 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 673

Compounds of the formula IF.5 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 674

Compounds of the formula IF.5 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 675

Compounds of the formula IF.5 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 676

Compounds of the formula IF.6 in which R^(A) is chlorine, Y¹′ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 677

Compounds of the formula IF.6 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 678

Compounds of the formula IF.6 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 679

Compounds of the formula IF.6 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 680

Compounds of the formula IF.6 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 681

Compounds of the formula IF.6 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 682

Compounds of the formula IF.6 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 683

Compounds of the formula IF.6 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 684

Compounds of the formula IF.6 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 685

Compounds of the formula IF.6 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 686

Compounds of the formula IF.6 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 687

Compounds of the formula IF.6 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 688

Compounds of the formula IF.6 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 689

Compounds of the formula IF.6 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 690

Compounds of the formula IF.6 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 691

Compounds of the formula IF.6 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 692

Compounds of the formula IF.6 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 693

Compounds of the formula IF.6 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 694

Compounds of the formula IF.7 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 695

Compounds of the formula IF.7 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 696

Compounds of the formula IF.7 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 697

Compounds of the formula IF.7 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 698

Compounds of the formula IF.7 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 699

Compounds of the formula IF.7 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 700

Compounds of the formula IF.7 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 701

Compounds of the formula IF.7 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 702

Compounds of the formula IF.7 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 703

Compounds of the formula IF.7 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 704

Compounds of the formula IF.7 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 705

Compounds of the formula IF.7 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 706

Compounds of the formula IF.7 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 707

Compounds of the formula IF.7 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 708

Compounds of the formula IF.7 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 709

Compounds of the formula IF.7 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 710

Compounds of the formula IF.7 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 711

Compounds of the formula IF.7 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 712

Compounds of the formula IF.8 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 713

Compounds of the formula IF.8 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 714

Compounds of the formula IF.8 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 715

Compounds of the formula IF.8 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 716

Compounds of the formula IF.8 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 717

Compounds of the formula IF.8 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 718

Compounds of the formula IF.8 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 719

Compounds of the formula IF. 8 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 720

Compounds of the formula IF.8 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 721

Compounds of the formula IF.8 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ orresponds for each compound to one row of Table B

Table 722

Compounds of the formula IF.8 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 723

Compounds of the formula IF.8 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 724

Compounds of the formula IF.8 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 725

Compounds of the formula IF.8 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 726

Compounds of the formula IF.8 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 727

Compounds of the formula IF.8 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 728

Compounds of the formula IF.8 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 729

Compounds of the formula IF.8 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 730

Compounds of the formula IF.9 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 731

Compounds of the formula IF.9 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 732

Compounds of the formula IF.9 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 733

Compounds of the formula IF.9 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 734

Compounds of the formula IF.9 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 735

Compounds of the formula IF.9 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 736

Compounds of the formula IF.9 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 737

Compounds of the formula IF.9 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 738

Compounds of the formula IF.9 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 739

Compounds of the formula IF.9 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 740

Compounds of the formula IF.9 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 741

Compounds of the formula IP.9 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 742

Compounds of the formula IF.9 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 743

Compounds of the formula IF.9 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 744

Compounds of the formula IF.9 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 745

Compounds of the formula IF.9 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 746

Compounds of the formula IF.9 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 747

Compounds of the formula IF.9 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 748

Compounds of the formula IF.10 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 749

Compounds of the formula IF.10 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 750

Compounds of the formula IF.10 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 751

Compounds of the formula IF.10 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 752

Compounds of the formula IF.10 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 753

Compounds of the formula IF.10 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 754

Compounds of the formula IF.10 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 755

Compounds of the formula IF.10 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 756

Compounds of the formula IF.10 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 757

Compounds of the formula IF.10 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 758

Compounds of the formula IF.10 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 759

Compounds of the formula IF.10 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 760

Compounds of the formula IF.10 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 761

Compounds of the formula IF.10 in which R^(A) is methoxy, Y¹′ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 762

Compounds of the formula IF.10 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 763

Compounds of the formula IF.10 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 764

Compounds of the formula IF.10 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 765

Compounds of the formula IF.10 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 766

Compounds of the formula IF.11 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 767

Compounds of the formula IF.11 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 768

Compounds of the formula IF.11 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 769

Compounds of the formula IF.11 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 770

Compounds of the formula IF.11 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 771

Compounds of the formula IF.11 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 772

Compounds of the formula IF.11 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 773

Compounds of the formula IF.11 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 774

Compounds of the formula IF.11 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 775

Compounds of the formula IF.11 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 776

Compounds of the formula IF.11 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 777

Compounds of the formula IF.11 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 778

Compounds of the formula IF.11 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 779

Compounds of the formula IF.11 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 780

Compounds of the formula IF.11 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 781

Compounds of the formula IF.11 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 782

Compounds of the formula IF.11 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 783

Compounds of the formula IF.11 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 784

Compounds of the formula IF.12 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 785

Compounds of the formula IF.12 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 786

Compounds of the formula IF.12 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 787

Compounds of the formula IF.12 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 788

Compounds of the formula IF.12 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 789

Compounds of the formula IF.12 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 790

Compounds of the formula IF.12 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 791

Compounds of the formula IF.12 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 792

Compounds of the formula IF.12 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 793

Compounds of the formula IF.12 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 794

Compounds of the formula IF.12 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 795

Compounds of the formula IF.12 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 796

Compounds of the formula IF.12 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 797

Compounds of the formula IF.12 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 798

Compounds of the formula IF.12 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 799

Compounds of the formula IF.12 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 800

Compounds of the formula IF.12 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 801

Compounds of the formula IF.12 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 802

Compounds of the formula IF.13 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 803

Compounds of the formula IF.13 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 804

Compounds of the formula IF.13 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 805

Compounds of the formula IF.13 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 806

Compounds of the formula IF.13 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 807

Compounds of the formula IF.13 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 808

Compounds of the formula IF.13 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 809

Compounds of the formula IF.13 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 810

Compounds of the formula IF.13 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 811

Compounds of the formula IF.13 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 812

Compounds of the formula IF.13 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 813

Compounds of the formula IF.13 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 814

Compounds of the formula IF.13 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 815

Compounds of the formula IF.13 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 816

Compounds of the formula IF.13 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 817

Compounds of the formula IF.13 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 818

Compounds of the formula IF.13 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 819

Compounds of the formula IF.13 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 820

Compounds of the formula IG.1 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 821

Compounds of the formula IG.1 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 822

Compounds of the formula IG.1 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 823

Compounds of the formula IG.1 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 824

Compounds of the formula IG.1 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 825

Compounds of the formula IG.1 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 826

Compounds of the formula IG.1 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 827

Compounds of the formula IG.1 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 828

Compounds of the formula IG.1 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 829

Compounds of the formula IG.1 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 830

Compounds of the formula IG.1 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 831

Compounds of the formula IG.1 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 832

Compounds of the formula IG.1 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 833

Compounds of the formula IG.1 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 834

Compounds of the formula IG.1 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 835

Compounds of the formula IG.1 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 836

Compounds of the formula IG.1 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 837

Compounds of the formula IG.1 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 838

Compounds of the formula IG.3 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 839

Compounds of the formula IG.3 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 840

Compounds of the formula IG.3 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 841

Compounds of the formula IG.3 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 842

Compounds of the formula IG.3 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 843

Compounds of the formula IG.3 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 844

Compounds of the formula IG.3 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 845

Compounds of the formula IG.3 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 846

Compounds of the formula IG.3 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 847

Compounds of the formula IG.3 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 848

Compounds of the formula IG.3 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 849

Compounds of the formula IG.3 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 850

Compounds of the formula IG.3 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 851

Compounds of the formula IG.3 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 852

Compounds of the formula IG.3 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 853

Compounds of the formula IG.3 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 854

Compounds of the formula IG.3 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 855

Compounds of the formula IG.3 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 856

Compounds of the formula IG.4 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 857

Compounds of the formula IG.4 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 858

Compounds of the formula IG.4 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 859

Compounds of the formula IG.4 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 860

Compounds of the formula IG.4 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 861

Compounds of the formula IG.4 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 862

Compounds of the formula IG.4 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 863

Compounds of the formula IG.4 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 864

Compounds of the formula IG.4 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 865

Compounds of the formula IG.4 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 866

Compounds of the formula IG.4 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 867

Compounds of the formula IG.4 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 868

Compounds of the formula IG.4 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 869

Compounds of the formula IG.4 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 870

Compounds of the formula IG.4 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 871

Compounds of the formula IG.4 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 872

Compounds of the formula IG.4 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 873

Compounds of the formula IG.4 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 874

Compounds of the formula IG.5 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 875

Compounds of the formula IG.5 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 876

Compounds of the formula IG.5 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 877

Compounds of the formula IG.5 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 878

Compounds of the formula IG.5 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 879

Compounds of the formula IG.5 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 880

Compounds of the formula IG.5 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 881

Compounds of the formula IG.5 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 882

Compounds of the formula IG.5 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 883

Compounds of the formula IG.5 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 884

Compounds of the formula IG.5 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 885

Compounds of the formula IG.5 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 886

Compounds of the formula IG.5 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 887

Compounds of the formula IG.5 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 888

Compounds of the formula IG.5 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 889

Compounds of the formula IG.5 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 890

Compounds of the formula IG.5 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 891

Compounds of the formula IG.5 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 892

Compounds of the formula IG.9 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 893

Compounds of the formula IG.9 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 894

Compounds of the formula IG.9 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 895

Compounds of the formula IG.9 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 896

Compounds of the formula IG.9 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 897

Compounds of the formula IG.9 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 898

Compounds of the formula IG.9 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 899

Compounds of the formula IG.9 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 900

Compounds of the formula IG.9 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 901

Compounds of the formula IG.9 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 902

Compounds of the formula IG.9 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table C

Table 903

Compounds of the formula IG.9 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 904

Compounds of the formula IG.9 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 905

Compounds of the formula IG.9 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 906

Compounds of the formula IG.9 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 907

Compounds of the formula IG.9 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 908

Compounds of the formula IG.9 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 909

Compounds of the formula IG.9 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 910

Compounds of the formula IG.10 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 911

Compounds of the formula IG.10 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 912

Compounds of the formula IG.10 in which R^(A) is chlorine, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 913

Compounds of the formula IG.10 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 914

Compounds of the formula IG.10 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 915

Compounds of the formula IG.10 in which R^(A) is chlorine, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 916

Compounds of the formula IG.10 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 917

Compounds of the formula IG.10 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 918

Compounds of the formula IG.10 in which R^(A) is methyl, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 919

Compounds of the formula IG.10 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 920

Compounds of the formula IG.10 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 921

Compounds of the formula IG.10 in which R^(A) is methyl, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 922

Compounds of the formula IG.10 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 923

Compounds of the formula IG.10 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 924

Compounds of the formula IG.10 in which R^(A) is methoxy, Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 925

Compounds of the formula IG.10 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 926

Compounds of the formula IG.10 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 927

Compounds of the formula IG.10 in which R^(A) is methoxy, Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 928

Compounds of the formula IH.1 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 929

Compounds of the formula IH.1 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 930

Compounds of the formula IH.1 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 931

Compounds of the formula IH.1 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 932

Compounds of the formula IH.1 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 933

Compounds of the formula IH.1 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 934

Compounds of the formula IH.2 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 935

Compounds of the formula IH.2 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 936

Compounds of the formula IH.2 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 937

Compounds of the formula IH.2 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 938

Compounds of the formula IH.2 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 939

Compounds of the formula IH.2 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 940

Compounds of the formula IH.3 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 941

Compounds of the formula IH.3 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 942

Compounds of the formula IH.3 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 943

Compounds of the formula IH.3 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 944

Compounds of the formula IH.3 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 945

Compounds of the formula IH.3 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 946

Compounds of the formula IH.4 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 947

Compounds of the formula IH.4 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 948

Compounds of the formula IH.4 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 949

Compounds of the formula IH.4 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 950

Compounds of the formula IH.4 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 951

Compounds of the formula IH.4 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 952

Compounds of the formula IH.5 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 953

Compounds of the formula IH.5 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 954

Compounds of the formula IH.5 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 955

Compounds of the formula IH.5 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 956

Compounds of the formula IH.5 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 957

Compounds of the formula IH.5 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 958

Compounds of the formula IH.6 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 959

Compounds of the formula IH.6 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 960

Compounds of the formula IH.6 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 961

Compounds of the formula IH.6 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 962

Compounds of the formula IH.6 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 963

Compounds of the formula IH.6 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 964

Compounds of the formula IH.7 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 965

Compounds of the formula IH.7 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 966

Compounds of the formula IH.7 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 967

Compounds of the formula IH.7 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 968

Compounds of the formula IH.7 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 969

Compounds of the formula IH.7 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 970

Compounds of the formula IH.8 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 971

Compounds of the formula IH.8 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 972

Compounds of the formula IH.8 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 973

Compounds of the formula IH.8 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 974

Compounds of the formula IH.8 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 975

Compounds of the formula IH.8 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R² and R³ corresponds for each compound to one row of Table B

Table 976

Compounds of the formula IH.9 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 977

Compounds of the formula IH.9 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 978

Compounds of the formula IH.9 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 979

Compounds of the formula IH.9 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 980

Compounds of the formula IH.9 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 981

Compounds of the formula IH.9 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹ and R² corresponds for each compound to one row of Table C

Table 982

Compounds of the formula IH.10 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 983

Compounds of the formula IH.10 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 984

Compounds of the formula IH.10 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 985

Compounds of the formula IH.10 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 986

Compounds of the formula IH.10 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 987

Compounds of the formula IH.10 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 988

Compounds of the formula IH.11 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 989

Compounds of the formula IH.11 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 990

Compounds of the formula IH.11 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 991

Compounds of the formula IH.11 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 992

Compounds of the formula IH.11 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 993

Compounds of the formula IH.11 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table D

Table 994

Compounds of the formula IH.12 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 995

Compounds of the formula IH.12 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 996

Compounds of the formula IH.12 in which Y¹ is chlorine, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 997

Compounds of the formula IH.12 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 998

Compounds of the formula IH.12 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 999

Compounds of the formula IH.12 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 1000

Compounds of the formula IH.13 in which Y¹ is chlorine, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 1001

Compounds of the formula IH.13 in which Y¹ is chlorine, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 1002

Compounds of the formula IH.13 in which Y¹ is chlorine, Ylf is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 1003

Compounds of the formula IH.13 in which Y¹ is methyl, Y¹′ is hydrogen and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 1004

Compounds of the formula IH.13 in which Y¹ is methyl, Y¹′ is chlorine and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

Table 1005

Compounds of the formula IH.13 in which Y¹ is methyl, Y¹′ is methyl and the combination of the radicals R¹, R² and R³ corresponds for each compound to one row of Table A

TABLE A No. R¹ R² R³ A-1 H H H A-2 F H H A-3 Cl H H A-4 Br H H A-5 CH₃ H H A-6 C₂H₅ H H A-7 n-C₃H₇ H H A-8 i-C₃H₇ H H A-9 CF₃ H H A-10 H F H A-11 F F H A-12 Cl F H A-13 Br F H A-14 CH₃ F H A-15 C₂H₅ F H A-16 n-C₃H₇ F H A-17 i-C₃H₇ F H A-18 CF₃ F H A-19 H Cl H A-20 F Cl H A-21 Cl Cl H A-22 Br Cl H A-23 CH₃ Cl H A-24 C₂H₅ Cl H A-25 n-C₃H₇ Cl H A-26 i-C₃H₇ Cl H A-27 CF₃ Cl H A-28 H Br H A-29 F Br H A-30 Cl Br H A-31 Br Br H A-32 CH₃ Br H A-33 C₂H₅ Br H A-34 n-C₃H₇ Br H A-35 i-C₃H₇ Br H A-36 CF₃ Br H A-37 H CH₃ H A-38 F CH₃ H A-39 Cl CH₃ H A-40 Br CH₃ H A-41 CH₃ CH₃ H A-42 C₂H₅ CH₃ H A-43 n-C₃H₇ CH₃ H A-44 i-C₃H₇ CH₃ H A-45 CF₃ CH₃ H A-46 H C₂H₅ H A-47 F C₂H₅ H A-48 Cl C₂H₅ H A-49 Br C₂H₅ H A-50 CH₃ C₂H₅ H A-51 C₂H₅ C₂H₅ H A-52 n-C₃H₇ C₂H₅ H A-53 i-C₃H₇ C₂H₅ H A-54 CF₃ C₂H₅ H A-55 H i-C₃H₇ H A-56 F i-C₃H₇ H A-57 Cl i-C₃H₇ H A-58 Br i-C₃H₇ H A-59 CH₃ i-C₃H₇ H A-60 C₂H₅ i-C₃H₇ H A-61 n-C₃H₇ i-C₃H₇ H A-62 i-C₃H₇ i-C₃H₇ H A-63 CF₃ i-C₃H₇ H A-64 CHF₂ i-C₃H₇ H A-65 CH₂F i-C₃H₇ H A-66 H CF₃ H A-67 F CF₃ H A-68 Cl CF₃ H A-69 Br CF₃ H A-70 CH₃ CF₃ H A-71 C₂H₅ CF₃ H A-72 n-C₃H₇ CF₃ H A-73 i-C₃H₇ CF₃ H A-74 CF₃ CF₃ H A-75 CHF₂ CF₃ H A-76 H H Cl A-77 F H Cl A-78 Cl H Cl A-79 Br H Cl A-80 CH₃ H Cl A-81 C₂H₅ H Cl A-82 n-C₃H₇ H Cl A-83 i-C₃H₇ H Cl A-84 CF₃ H Cl A-85 H F Cl A-86 F F Cl A-87 Cl F Cl A-88 Br F Cl A-89 CH₃ F Cl A-90 C₂H₅ F Cl A-91 n-C₃H₇ F Cl A-92 i-C₃H₇ F Cl A-93 CF₃ F Cl A-94 H Cl Cl A-95 F Cl Cl A-96 Cl Cl Cl A-97 Br Cl Cl A-98 CH₃ Cl Cl A-99 C₂H₅ Cl Cl A-100 n-C₃H₇ Cl Cl A-101 i-C₃H₇ Cl Cl A-102 CF₃ Cl Cl A-103 H Br Cl A-104 F Br Cl A-105 Cl Br Cl A-106 Br Br Cl A-107 CH₃ Br Cl A-108 C₂H₅ Br Cl A-109 n-C₃H₇ Br Cl A-110 i-C₃H₇ Br Cl A-111 CF₃ Br Cl A-112 H CH₃ Cl A-113 F CH₃ Cl A-114 Cl CH₃ Cl A-115 Br CH₃ Cl A-116 CH₃ CH₃ Cl A-117 C₂H₅ CH₃ Cl A-118 n-C₃H₇ CH₃ Cl A-119 i-C₃H₇ CH₃ Cl A-120 CF₃ CH₃ Cl A-121 H C₂H₅ Cl A-122 F C₂H₅ Cl A-123 Cl C₂H₅ Cl A-124 Br C₂H₅ Cl A-125 CH₃ C₂H₅ Cl A-126 C₂H₅ C₂H₅ Cl A-127 n-C₃H₇ C₂H₅ Cl A-128 i-C₃H₇ C₂H₅ Cl A-129 CF₃ C₂H₅ Cl A-130 H i-C₃H₇ Cl A-131 F i-C₃H₇ Cl A-132 Cl i-C₃H₇ Cl A-133 Br i-C₃H₇ Cl A-134 CH₃ i-C₃H₇ Cl A-135 C₂H₅ i-C₃H₇ Cl A-136 n-C₃H₇ i-C₃H₇ Cl A-137 i-C₃H₇ i-C₃H₇ Cl A-138 CF₃ i-C₃H₇ Cl A-139 CHF₂ i-C₃H₇ Cl A-140 CH₂F i-C₃H₇ Cl A-141 H CF₃ Cl A-142 F CF₃ Cl A-143 Cl CF₃ Cl A-144 Br CF₃ Cl A-145 CH₃ CF₃ Cl A-146 C₂H₅ CF₃ Cl A-147 n-C₃H₇ CF₃ Cl A-148 i-C₃H₇ CF₃ Cl A-149 CF₃ CF₃ Cl A-150 CHF₂ CF₃ Cl A-151 H H CH₃ A-152 F H CH₃ A-153 Cl H CH₃ A-154 Br H CH₃ A-155 CH₃ H CH₃ A-156 C₂H₅ H CH₃ A-157 n-C₃H₇ H CH₃ A-158 i-C₃H₇ H CH₃ A-159 CF₃ H CH₃ A-160 H F CH₃ A-161 F F CH₃ A-162 Cl F CH₃ A-163 Br F CH₃ A-164 CH₃ F CH₃ A-165 C₂H₅ F CH₃ A-166 n-C₃H₇ F CH₃ A-167 i-C₃H₇ F CH₃ A-168 CF₃ F CH₃ A-169 H Cl CH₃ A-170 F Cl CH₃ A-171 Cl Cl CH₃ A-172 Br Cl CH₃ A-173 CH₃ Cl CH₃ A-174 C₂H₅ Cl CH₃ A-175 n-C₃H₇ Cl CH₃ A-176 i-C₃H₇ Cl CH₃ A-177 CF₃ Cl CH₃ A-178 H Br CH₃ A-179 F Br CH₃ A-180 Cl Br CH₃ A-181 Br Br CH₃ A-182 CH₃ Br CH₃ A-183 C₂H₅ Br CH₃ A-184 n-C₃H₇ Br CH₃ A-185 i-C₃H₇ Br CH₃ A-186 CF₃ Br CH₃ A-187 H CH₃ CH₃ A-188 F CH₃ CH₃ A-189 Cl CH₃ CH₃ A-190 Br CH₃ CH₃ A-191 CH₃ CH₃ CH₃ A-192 C₂H₅ CH₃ CH₃ A-193 n-C₃H₇ CH₃ CH₃ A-194 i-C₃H₇ CH₃ CH₃ A-195 CF₃ CH₃ CH₃ A-196 H C₂H₅ CH₃ A-197 F C₂H₅ CH₃ A-198 Cl C₂H₅ CH₃ A-199 Br C₂H₅ CH₃ A-200 CH₃ C₂H₅ CH₃ A-201 C₂H₅ C₂H₅ CH₃ A-202 n-C₃H₇ C₂H₅ CH₃ A-203 i-C₃H₇ C₂H₅ CH₃ A-204 CF₃ C₂H₅ CH₃ A-205 H i-C₃H₇ CH₃ A-206 F i-C₃H₇ CH₃ A-207 Cl i-C₃H₇ CH₃ A-208 Br i-C₃H₇ CH₃ A-209 CH₃ i-C₃H₇ CH₃ A-210 C₂H₅ i-C₃H₇ CH₃ A-211 n-C₃H₇ i-C₃H₇ CH₃ A-212 i-C₃H₇ i-C₃H₇ CH₃ A-213 CF₃ i-C₃H₇ CH₃ A-214 CHF₂ i-C₃H₇ CH₃ A-215 CH₂F i-C₃H₇ CH₃ A-216 H CF₃ CH₃ A-217 F CF₃ CH₃ A-218 Cl CF₃ CH₃ A-219 Br CF₃ CH₃ A-220 CH₃ CF₃ CH₃ A-221 C₂H₅ CF₃ CH₃ A-222 n-C₃H₇ CF₃ CH₃ A-223 i-C₃H₇ CF₃ CH₃ A-224 CF₃ CF₃ CH₃ A-225 CHF₂ CF₃ CH₃ A-226 H H i-C₃H₇ A-227 F H i-C₃H₇ A-228 Cl H i-C₃H₇ A-229 Br H i-C₃H₇ A-230 CH₃ H i-C₃H₇ A-231 C₂H₅ H i-C₃H₇ A-232 n-C₃H₇ H i-C₃H₇ A-233 i-C₃H₇ H i-C₃H₇ A-234 CF₃ H i-C₃H₇ A-235 H F i-C₃H₇ A-236 F F i-C₃H₇ A-237 Cl F i-C₃H₇ A-238 Br F i-C₃H₇ A-239 CH₃ F i-C₃H₇ A-240 C₂H₅ F i-C₃H₇ A-241 n-C₃H₇ F i-C₃H₇ A-242 i-C₃H₇ F i-C₃H₇ A-243 CF₃ F i-C₃H₇ A-244 H Cl i-C₃H₇ A-245 F Cl i-C₃H₇ A-246 Cl Cl i-C₃H₇ A-247 Br Cl i-C₃H₇ A-248 CH₃ Cl i-C₃H₇ A-249 C₂H₅ Cl i-C₃H₇ A-250 n-C₃H₇ Cl i-C₃H₇ A-251 i-C₃H₇ Cl i-C₃H₇ A-252 CF₃ Cl i-C₃H₇ A-253 H Br i-C₃H₇ A-254 F Br i-C₃H₇ A-255 Cl Br i-C₃H₇ A-256 Br Br i-C₃H₇ A-257 CH₃ Br i-C₃H₇ A-258 C₂H₅ Br i-C₃H₇ A-259 n-C₃H₇ Br i-C₃H₇ A-260 i-C₃H₇ Br i-C₃H₇ A-261 CF₃ Br i-C₃H₇ A-262 H CH₃ i-C₃H₇ A-263 F CH₃ i-C₃H₇ A-264 Cl CH₃ i-C₃H₇ A-265 Br CH₃ i-C₃H₇ A-266 CH₃ CH₃ i-C₃H₇ A-267 C₂H₅ CH₃ i-C₃H₇ A-268 n-C₃H₇ CH₃ i-C₃H₇ A-269 i-C₃H₇ CH₃ i-C₃H₇ A-270 CF₃ CH₃ i-C₃H₇ A-271 H C₂H₅ i-C₃H₇ A-272 F C₂H₅ i-C₃H₇ A-273 Cl C₂H₅ i-C₃H₇ A-274 Br C₂H₅ i-C₃H₇ A-275 CH₃ C₂H₅ i-C₃H₇ A-276 C₂H₅ C₂H₅ i-C₃H₇ A-277 n-C₃H₇ C₂H₅ i-C₃H₇ A-278 i-C₃H₇ C₂H₅ i-C₃H₇ A-279 CF₃ C₂H₅ i-C₃H₇ A-280 H i-C₃H₇ i-C₃H₇ A-281 F i-C₃H₇ i-C₃H₇ A-282 Cl i-C₃H₇ i-C₃H₇ A-283 Br i-C₃H₇ i-C₃H₇ A-284 CH₃ i-C₃H₇ i-C₃H₇ A-285 C₂H₅ i-C₃H₇ i-C₃H₇ A-286 n-C₃H₇ i-C₃H₇ i-C₃H₇ A-287 i-C₃H₇ i-C₃H₇ i-C₃H₇ A-288 CF₃ i-C₃H₇ i-C₃H₇ A-289 CHF₂ i-C₃H₇ i-C₃H₇ A-290 CH₂F i-C₃H₇ i-C₃H₇ A-291 H CF₃ i-C₃H₇ A-292 F CF₃ i-C₃H₇ A-293 Cl CF₃ i-C₃H₇ A-294 Br CF₃ i-C₃H₇ A-295 CH₃ CF₃ i-C₃H₇ A-296 C₂H₅ CF₃ i-C₃H₇ A-297 n-C₃H₇ CF₃ i-C₃H₇ A-298 i-C₃H₇ CF₃ i-C₃H₇ A-299 CF₃ CF₃ i-C₃H₇ A-300 CHF₂ CF₃ i-C₃H₇ A-301 H H CF₃ A-302 F H CF₃ A-303 Cl H CF₃ A-304 Br H CF₃ A-305 CH₃ H CF₃ A-306 C₂H₅ H CF₃ A-307 n-C₃H₇ H CF₃ A-308 i-C₃H₇ H CF₃ A-309 CF₃ H CF₃ A-310 H F CF₃ A-311 F F CF₃ A-312 Cl F CF₃ A-313 Br F CF₃ A-314 CH₃ F CF₃ A-315 C₂H₅ F CF₃ A-316 n-C₃H₇ F CF₃ A-317 i-C₃H₇ F CF₃ A-318 CF₃ F CF₃ A-319 H Cl CF₃ A-320 F Cl CF₃ A-321 Cl Cl CF₃ A-322 Br Cl CF₃ A-323 CH₃ Cl CF₃ A-324 C₂H₅ Cl CF₃ A-325 n-C₃H₇ Cl CF₃ A-326 i-C₃H₇ Cl CF₃ A-327 CF₃ Cl CF₃ A-328 H Br CF₃ A-329 F Br CF₃ A-330 Cl Br CF₃ A-331 Br Br CF₃ A-332 CH₃ Br CF₃ A-333 C₂H₅ Br CF₃ A-334 n-C₃H₇ Br CF₃ A-335 i-C₃H₇ Br CF₃ A-336 CF₃ Br CF₃ A-337 H CH₃ CF₃ A-338 F CH₃ CF₃ A-339 Cl CH₃ CF₃ A-340 Br CH₃ CF₃ A-341 CH₃ CH₃ CF₃ A-342 C₂H₅ CH₃ CF₃ A-343 n-C₃H₇ CH₃ CF₃ A-344 i-C₃H₇ CH₃ CF₃ A-345 CF₃ CH₃ CF₃ A-346 H C₂H₅ CF₃ A-347 F C₂H₅ CF₃ A-348 Cl C₂H₅ CF₃ A-349 Br C₂H₅ CF₃ A-350 CH₃ C₂H₅ CF₃ A-351 C₂H₅ C₂H₅ CF₃ A-352 n-C₃H₇ C₂H₅ CF₃ A-353 i-C₃H₇ C₂H₅ CF₃ A-354 CF₃ C₂H₅ CF₃ A-355 H i-C₃H₇ CF₃ A-356 F i-C₃H₇ CF₃ A-357 Cl i-C₃H₇ CF₃ A-358 Br i-C₃H₇ CF₃ A-359 CH₃ i-C₃H₇ CF₃ A-360 C₂H₅ i-C₃H₇ CF₃ A-361 n-C₃H₇ i-C₃H₇ CF₃ A-362 i-C₃H₇ i-C₃H₇ CF₃ A-363 CF₃ i-C₃H₇ CF₃ A-364 CHF₂ i-C₃H₇ CF₃ A-365 CH₂F i-C₃H₇ CF₃ A-366 H CF₃ CF₃ A-367 F CF₃ CF₃ A-368 Cl CF₃ CF₃ A-369 Br CF₃ CF₃ A-370 CH₃ CF₃ CF₃ A-371 C₂H₅ CF₃ CF₃ A-372 n-C₃H₇ CF₃ CF₃ A-373 i-C₃H₇ CF₃ CF₃ A-374 CF₃ CF₃ CF₃ A-375 CHF₂ CF₃ CF₃

TABLE B No. R² R³ B-1 H H B-2 F H B-3 Cl H B-4 Br H B-5 CH₃ H B-6 C₂H₅ H B-7 n-C₃H₇ H B-8 i-C₃H₇ H B-9 CF₃ H B-10 H F B-11 F F B-12 Cl F B-13 Br F B-14 CH₃ F B-15 C₂H₅ F B-16 n-C₃H₇ F B-17 i-C₃H₇ F B-18 CF₃ F B-19 H Cl B-20 F Cl B-21 Cl Cl B-22 Br Cl B-23 CH₃ Cl B-24 C₂H₅ Cl B-25 n-C₃H₇ Cl B-26 i-C₃H₇ Cl B-27 H Br B-28 F Br B-29 Cl Br B-30 Br Br B-31 CH₃ Br B-32 C₂H₅ Br B-33 n-C₃H₇ Br B-34 i-C₃H₇ Br B-35 CF₃ Br B-36 H CH₃ B-37 F CH₃ B-38 Cl CH₃ B-39 Br CH₃ B-40 CH₃ CH₃ B-41 C₂H₅ CH₃ B-42 n-C₃H₇ CH₃ B-43 i-C₃H₇ CH₃ B-44 CF₃ CH₃ B-45 H C₂H₅ B-46 F C₂H₅ B-47 Cl C₂H₅ B-48 Br C₂H₅ B-49 CH₃ C₂H₅ B-50 C₂H₅ C₂H₅ B-51 n-C₃H₇ C₂H₅ B-52 i-C₃H₇ C₂H₅ B-53 CF₃ C₂H₅ B-54 H i-C₃H₇ B-55 F i-C₃H₇ B-56 Cl i-C₃H₇ B-57 Br i-C₃H₇ B-58 CH₃ i-C₃H₇ B-59 C₂H₅ i-C₃H₇ B-60 n-C₃H₇ i-C₃H₇ B-61 i-C₃H₇ i-C₃H₇ B-62 CF₃ i-C₃H₇ B-63 CHF₂ i-C₃H₇ B-64 CH₂F i-C₃H₇ B-65 H CF₃ B-66 F CF₃ B-67 Cl CF₃ B-68 Br CF₃ B-69 CH₃ CF₃ B-70 C₂H₅ CF₃ B-71 n-C₃H₇ CF₃ B-72 i-C₃H₇ CF₃ B-73 CF₃ CF₃ B-74 CHF₂ CF₃

TABLE C No. R¹ R² C-1 H H C-2 F H C-3 Cl H C-4 Br H C-5 CH₃ H C-6 C₂H₅ H C-7 n-C₃H₇ H C-8 i-C₃H₇ H C-9 CF₃ H C-10 H F C-11 F F C-12 Cl F C-13 Br F C-14 CH₃ F C-15 C₂H₅ F C-16 n-C₃H₇ F C-17 i-C₃H₇ F C-18 CF₃ F C-19 H Cl C-20 F Cl C-21 Cl Cl C-22 Br Cl C-23 CH₃ Cl C-24 C₂H₅ Cl C-25 n-C₃H₇ Cl C-26 i-C₃H₇ Cl C-27 CF₃ Cl C-28 H Br C-29 F Br C-30 Cl Br C-31 Br Br C-32 CH₃ Br C-33 C₂H₅ Br C-34 n-C₃H₇ Br C-35 i-C₃H₇ Br C-36 CF₃ Br C-37 H CH₃ C-38 F CH₃ C-39 Cl CH₃ C-40 Br CH₃ C-41 CH₃ CH₃ C-42 C₂H₅ CH₃ C-43 n-C₃H₇ CH₃ C-44 i-C₃H₇ CH₃ C-45 CF₃ CH₃ C-46 H C₂H₅ C-47 F C₂H₅ C-48 Cl C₂H₅ C-49 Br C₂H₅ C-50 CH₃ C₂H₅ C-51 C₂H₅ C₂H₅ C-52 n-C₃H₇ C₂H₅ C-53 i-C₃H₇ C₂H₅ C-54 CF₃ C₂H₅ C-55 H i-C₃H₇ C-56 F i-C₃H₇ C-57 Cl i-C₃H₇ C-58 Br i-C₃H₇ C-59 CH₃ i-C₃H₇ C-60 C₂H₅ i-C₃H₇ C-61 n-C₃H₇ i-C₃H₇ C-62 i-C₃H₇ i-C₃H₇ C-63 CF₃ i-C₃H₇ C-64 CHF₂ i-C₃H₇ C-65 CH₂F i-C₃H₇ C-66 H CF₃ C-67 F CF₃ C-68 Cl CF₃ C-69 Br CF₃ C-70 CH₃ CF₃ C-71 C₂H₅ CF₃ C-72 n-C₃H₇ CF₃ C-73 i-C₃H₇ CF₃ C-74 CF₃ CF₃ C-75 CHF₂ CF₃

TABLE D No. R¹ R² R³ D-1 H H H D-2 F H H D-3 Cl H H D-4 Br H H D-5 CH₃ H H D-6 C₂H₅ H H D-7 n-C₃H₇ H H D-8 i-C₃H₇ H H D-9 CF₃ H H D-10 H F H D-11 F F H D-12 Cl F H D-13 Br F H D-14 CH₃ F H D-15 C₂H₅ F H D-16 n-C₃H₇ F H D-17 i-C₃H₇ F H D-18 CF₃ F H D-19 H Cl H D-20 F Cl H D-21 Cl Cl H D-22 Br Cl H D-23 CH₃ Cl H D-24 C₂H₅ Cl H D-25 n-C₃H₇ Cl H D-26 CF₃ Cl H D-27 H Br H D-28 F Br H D-29 Cl Br H D-30 Br Br H D-31 CH₃ Br H D-32 C₂H₅ Br H D-33 n-C₃H₇ Br H D-34 i-C₃H₇ Br H D-35 CF₃ Br H D-36 H CH₃ H D-37 F CH₃ H D-38 Cl CH₃ H D-39 Br CH₃ H D-40 CH₃ CH₃ H D-41 C₂H₅ CH₃ H D-42 n-C₃H₇ CH₃ H D-43 i-C₃H₇ CH₃ H D-44 CF₃ CH₃ H D-45 H C₂H₅ H D-46 F C₂H₅ H D-47 Cl C₂H₅ H D-48 Br C₂H₅ H D-49 CH₃ C₂H₅ H D-50 C₂H₅ C₂H₅ H D-51 n-C₃H₇ C₂H₅ H D-52 i-C₃H₇ C₂H₅ H D-53 CF₃ C₂H₅ H D-54 H i-C₃H₇ H D-55 F i-C₃H₇ H D-56 Cl i-C₃H₇ H D-57 Br i-C₃H₇ H D-58 CH₃ i-C₃H₇ H D-59 C₂H₅ i-C₃H₇ H D-60 n-C₃H₇ i-C₃H₇ H D-61 i-C₃H₇ i-C₃H₇ H D-62 CF₃ i-C₃H₇ H D-63 CHF₂ i-C₃H₇ H D-64 CH₂F i-C₃H₇ H D-65 CHF₂ t-C₄H₉ H D-66 H CF₃ H D-67 F CF₃ H D-68 Cl CF₃ H D-69 Br CF₃ H D-70 CH₃ CF₃ H D-71 C₂H₅ CF₃ H D-72 n-C₃H₇ CF₃ H D-73 i-C₃H₇ CF₃ H D-74 CF₃ CF₃ H D-75 CHF₂ CF₃ H D-76 H H F D-77 F H F D-78 Cl H F D-79 Br H F D-80 CH₃ H F D-81 C₂H₅ H F D-82 n-C₃H₇ H F D-83 i-C₃H₇ H F D-84 CF₃ H F D-85 H F F D-86 F F F D-87 Cl F F D-88 Br F F D-89 CH₃ F F D-90 C₂H₅ F F D-91 n-C₃H₇ F F D-92 i-C₃H₇ F F D-93 CF₃ F F D-94 H Cl F D-95 F Cl F D-96 Cl Cl F D-97 Br Cl F D-98 CH₃ Cl F D-99 C₂H₅ Cl F D-100 n-C₃H₇ Cl F D-101 i-C₃H₇ Cl F D-102 CF₃ Cl F D-103 H Br F D-104 F Br F D-105 Cl Br F D-106 Br Br F D-107 CH₃ Br F D-108 C₂H₅ Br F D-109 n-C₃H₇ Br F D-110 i-C₃H₇ Br F D-111 CF₃ Br F D-112 H CH₃ F D-113 F CH₃ F D-114 Cl CH₃ F D-115 Br CH₃ F D-116 CH₃ CH₃ F D-117 C₂H₅ CH₃ F D-118 n-C₃H₇ CH₃ F D-119 i-C₃H₇ CH₃ F D-120 CF₃ CH₃ F D-121 H C₂H₅ F D-122 F C₂H₅ F D-123 Cl C₂H₅ F D-124 Br C₂H₅ F D-125 CH₃ C₂H₅ F D-126 C₂H₅ C₂H₅ F D-127 n-C₃H₇ C₂H₅ F D-128 i-C₃H₇ C₂H₅ F D-129 CF₃ C₂H₅ F D-130 H i-C₃H₇ F D-131 F i-C₃H₇ F D-132 Cl i-C₃H₇ F D-133 Br i-C₃H₇ F D-134 CH₃ i-C₃H₇ F D-135 C₂H₅ i-C₃H₇ F D-136 n-C₃H₇ i-C₃H₇ F D-137 i-C₃H₇ i-C₃H₇ F D-138 CF₃ i-C₃H₇ F D-139 CHF₂ i-C₃H₇ F D-140 CH₂F i-C₃H₇ F D-141 H CF₃ F D-142 F CF₃ F D-143 Cl CF₃ F D-144 Br CF₃ F D-145 CH₃ CF₃ F D-146 C₂H₅ CF₃ F D-147 n-C₃H₇ CF₃ F D-148 i-C₃H₇ CF₃ F D-149 CF₃ CF₃ F D-150 CHF₂ CF₃ F D-151 H H Cl D-152 F H Cl D-153 Cl H Cl D-154 Br H Cl D-155 CH₃ H Cl D-156 C₂H₅ H Cl D-157 n-C₃H₇ H Cl D-158 i-C₃H₇ H Cl D-159 CF₃ H Cl D-160 H F Cl D-161 F F Cl D-162 Cl F Cl D-163 Br F Cl D-164 CH₃ F Cl D-165 C₂H₅ F Cl D-166 n-C₃H₇ F Cl D-167 i-C₃H₇ F Cl D-168 CF₃ F Cl D-169 H Cl Cl D-170 F Cl Cl D-171 Cl Cl Cl D-172 Br Cl Cl D-173 CH₃ Cl Cl D-174 C₂H₅ Cl Cl D-175 n-C₃H₇ Cl Cl D-176 i-C₃H₇ Cl Cl D-177 CF₃ Cl Cl D-178 H Br Cl D-179 F Br Cl D-180 Cl Br Cl D-181 Br Br Cl D-182 CH₃ Br Cl D-183 C₂H₅ Br Cl D-184 n-C₃H₇ Br Cl D-185 i-C₃H₇ Br Cl D-186 CF₃ Br Cl D-187 H CH₃ Cl D-188 F CH₃ Cl D-189 Cl CH₃ Cl D-190 Br CH₃ Cl D-191 CH₃ CH₃ Cl D-192 C₂H₅ CH₃ Cl D-193 n-C₃H₇ CH₃ Cl D-194 i-C₃H₇ CH₃ Cl D-195 CF₃ CH₃ Cl D-196 H C₂H₅ Cl D-197 F C₂H₅ Cl D-198 Cl C₂H₅ Cl D-199 Br C₂H₅ Cl D-200 CH₃ C₂H₅ Cl D-201 C₂H₅ C₂H₅ Cl D-202 n-C₃H₇ C₂H₅ Cl D-203 i-C₃H₇ C₂H₅ Cl D-204 CF₃ C₂H₅ Cl D-205 H i-C₃H₇ Cl D-206 F i-C₃H₇ Cl D-207 Cl i-C₃H₇ Cl D-208 Br i-C₃H₇ Cl D-209 CH₃ i-C₃H₇ Cl D-210 C₂H₅ i-C₃H₇ Cl D-211 n-C₃H₇ i-C₃H₇ Cl D-212 i-C₃H₇ i-C₃H₇ Cl D-213 CF₃ i-C₃H₇ Cl D-214 CHF₂ i-C₃H₇ Cl D-215 CH₂F i-C₃H₇ Cl D-216 H CF₃ Cl D-217 F CF₃ Cl D-218 Cl CF₃ Cl D-219 Br CF₃ Cl D-220 CH₃ CF₃ Cl D-221 C₂H₅ CF₃ Cl D-222 n-C₃H₇ CF₃ Cl D-223 i-C₃H₇ CF₃ Cl D-224 CF₃ CF₃ Cl D-225 CHF₂ CF₃ Cl D-226 H H Br D-227 F H Br D-228 Cl H Br D-229 Br H Br D-230 CH₃ H Br D-231 C₂H₅ H Br D-232 n-C₃H₇ H Br D-233 i-C₃H₇ H Br D-234 CF₃ H Br D-235 H F Br D-236 F F Br D-237 Cl F Br D-238 Br F Br D-239 CH₃ F Br D-240 C₂H₅ F Br D-241 n-C₃H₇ F Br D-242 i-C₃H₇ F Br D-243 CF₃ F Br D-244 H Cl Br D-245 F Cl Br D-246 Cl Cl Br D-247 Br Cl Br D-248 CH₃ Cl Br D-249 C₂H₅ Cl Br D-250 n-C₃H₇ Cl Br D-251 i-C₃H₇ Cl Br D-252 CF₃ Cl Br D-253 H Br Br D-254 F Br Br D-255 Cl Br Br D-256 Br Br Br D-257 CH₃ Br Br D-258 C₂H₅ Br Br D-259 n-C₃H₇ Br Br D-260 i-C₃H₇ Br Br D-261 CF₃ Br Br D-262 H CH₃ Br D-263 F CH₃ Br D-264 Cl CH₃ Br D-265 Br CH₃ Br D-266 CH₃ CH₃ Br D-267 C₂H₅ CH₃ Br D-268 n-C₃H₇ CH₃ Br D-269 i-C₃H₇ CH₃ Br D-270 CF₃ CH₃ Br D-271 H C₂H₅ Br D-272 F C₂H₅ Br D-273 Cl C₂H₅ Br D-274 Br C₂H₅ Br D-275 CH₃ C₂H₅ Br D-276 C₂H₅ C₂H₅ Br D-277 n-C₃H₇ C₂H₅ Br D-278 i-C₃H₇ C₂H₅ Br D-279 CF₃ C₂H₅ Br D-280 H i-C₃H₇ Br D-281 F i-C₃H₇ Br D-282 Cl i-C₃H₇ Br D-283 Br i-C₃H₇ Br D-284 CH₃ i-C₃H₇ Br D-285 C₂H₅ i-C₃H₇ Br D-286 n-C₃H₇ i-C₃H₇ Br D-287 i-C₃H₇ i-C₃H₇ Br D-288 CF₃ i-C₃H₇ Br D-289 CHF₂ i-C₃H₇ Br D-290 CH₂F i-C₃H₇ Br D-291 H CF₃ Br D-292 F CF₃ Br D-293 Cl CF₃ Br D-294 Br CF₃ Br D-295 CH₃ CF₃ Br D-296 C₂H₅ CF₃ Br D-297 n-C₃H₇ CF₃ Br D-298 i-C₃H₇ CF₃ Br D-299 CF₃ CF₃ Br D-300 CHF₂ CF₃ Br D-301 H H CH₃ D-302 F H CH₃ D-303 Cl H CH₃ D-304 Br H CH₃ D-305 CH₃ H CH₃ D-306 C₂H₅ H CH₃ D-307 n-C₃H₇ H CH₃ D-308 i-C₃H₇ H CH₃ D-309 s-C₄H₉ H CH₃ D-310 i-C₄H₉ H CH₃ D-311 t-C₄H₉ H CH₃ D-312 n-C₅H₁₁ H CH₃ D-313 CF₃ H CH₃ D-314 H F CH₃ D-315 F F CH₃ D-316 Cl F CH₃ D-317 Br F CH₃ D-318 CH₃ F CH₃ D-319 C₂H₅ F CH₃ D-320 n-C₃H₇ F CH₃ D-321 i-C₃H₇ F CH₃ D-322 CF₃ F CH₃ D-323 H Cl CH₃ D-324 F Cl CH₃ D-325 Cl Cl CH₃ D-326 Br Cl CH₃ D-327 CH₃ Cl CH₃ D-328 C₂H₅ Cl CH₃ D-329 n-C₃H₇ Cl CH₃ D-330 i-C₃H₇ Cl CH₃ D-331 CF₃ Cl CH₃ D-332 H Br CH₃ D-333 F Br CH₃ D-334 Cl Br CH₃ D-335 Br Br CH₃ D-336 CH₃ Br CH₃ D-337 C₂H₅ Br CH₃ D-338 n-C₃H₇ Br CH₃ D-339 i-C₃H₇ Br CH₃ D-340 s-C₄H₉ Br CH₃ D-341 CF₃ Br CH₃ D-342 H CH₃ CH₃ D-343 F CH₃ CH₃ D-344 Cl CH₃ CH₃ D-345 Br CH₃ CH₃ D-346 CH₃ CH₃ CH₃ D-347 C₂H₅ CH₃ CH₃ D-348 n-C₃H₇ CH₃ CH₃ D-349 i-C₃H₇ CH₃ CH₃ D-350 CF₃ CH₃ CH₃ D-351 H C₂H₅ CH₃ D-352 F C₂H₅ CH₃ D-353 Cl C₂H₅ CH₃ D-354 Br C₂H₅ CH₃ D-355 CH₃ C₂H₅ CH₃ D-356 C₂H₅ C₂H₅ CH₃ D-357 n-C₃H₇ C₂H₅ CH₃ D-358 i-C₃H₇ C₂H₅ CH₃ D-359 CF₃ C₂H₅ CH₃ D-360 H i-C₃H₇ CH₃ D-361 F i-C₃H₇ CH₃ D-362 Cl i-C₃H₇ CH₃ D-363 Br i-C₃H₇ CH₃ D-364 CH₃ i-C₃H₇ CH₃ D-365 C₂H₅ i-C₃H₇ CH₃ D-366 n-C₃H₇ i-C₃H₇ CH₃ D-367 i-C₃H₇ i-C₃H₇ CH₃ D-368 CF₃ i-C₃H₇ CH₃ D-369 CHF₂ i-C₃H₇ CH₃ D-370 CH₂F i-C₃H₇ CH₃ D-371 H CF₃ CH₃ D-372 F CF₃ CH₃ D-373 Cl CF₃ CH₃ D-374 Br CF₃ CH₃ D-375 CH₃ CF₃ CH₃ D-376 C₂H₅ CF₃ CH₃ D-377 n-C₃H₇ CF₃ CH₃ D-378 i-C₃H₇ CF₃ CH₃ D-379 CF₃ CF₃ CH₃ D-380 CHF₂ CF₃ CH₃ D-381 H H C₂H₅ D-382 F H C₂H₅ D-383 Cl H C₂H₅ D-384 Br H C₂H₅ D-385 CH₃ H C₂H₅ D-386 C₂H₅ H C₂H₅ D-387 n-C₃H₇ H C₂H₅ D-388 i-C₃H₇ H C₂H₅ D-389 CF₃ H C₂H₅ D-390 H F C₂H₅ D-391 F F C₂H₅ D-392 Cl F C₂H₅ D-393 Br F C₂H₅ D-394 CH₃ F C₂H₅ D-395 C₂H₅ F C₂H₅ D-396 n-C₃H₇ F C₂H₅ D-397 i-C₃H₇ F C₂H₅ D-398 CF₃ F C₂H₅ D-399 H Cl C₂H₅ D-400 F Cl C₂H₅ D-401 Cl Cl C₂H₅ D-402 Br Cl C₂H₅ D-403 CH₃ Cl C₂H₅ D-404 C₂H₅ Cl C₂H₅ D-405 n-C₃H₇ Cl C₂H₅ D-406 i-C₃H₇ Cl C₂H₅ D-407 CF₃ Cl C₂H₅ D-408 H Br C₂H₅ D-409 F Br C₂H₅ D-410 Cl Br C₂H₅ D-411 Br Br C₂H₅ D-412 CH₃ Br C₂H₅ D-413 C₂H₅ Br C₂H₅ D-414 n-C₃H₇ Br C₂H₅ D-415 i-C₃H₇ Br C₂H₅ D-416 CF₃ Br C₂H₅ D-417 H CH₃ C₂H₅ D-418 F CH₃ C₂H₅ D-419 Cl CH₃ C₂H₅ D-420 Br CH₃ C₂H₅ D-421 CH₃ CH₃ C₂H₅ D-422 C₂H₅ CH₃ C₂H₅ D-423 n-C₃H₇ CH₃ C₂H₅ D-424 i-C₃H₇ CH₃ C₂H₅ D-425 CF₃ CH₃ C₂H₅ D-426 H C₂H₅ C₂H₅ D-427 F C₂H₅ C₂H₅ D-428 Cl C₂H₅ C₂H₅ D-429 Br C₂H₅ C₂H₅ D-430 CH₃ C₂H₅ C₂H₅ D-431 C₂H₅ C₂H₅ C₂H₅ D-432 n-C₃H₇ C₂H₅ C₂H₅ D-433 i-C₃H₇ C₂H₅ C₂H₅ D-434 CF₃ C₂H₅ C₂H₅ D-435 H i-C₃H₇ C₂H₅ D-436 F i-C₃H₇ C₂H₅ D-437 Cl i-C₃H₇ C₂H₅ D-438 Br i-C₃H₇ C₂H₅ D-439 CH₃ i-C₃H₇ C₂H₅ D-440 C₂H₅ i-C₃H₇ C₂H₅ D-441 n-C₃H₇ i-C₃H₇ C₂H₅ D-442 i-C₃H₇ i-C₃H₇ C₂H₅ D-443 CF₃ i-C₃H₇ C₂H₅ D-444 CHF₂ i-C₃H₇ C₂H₅ D-445 CH₂F i-C₃H₇ C₂H₅ D-446 H CF₃ C₂H₅ D-447 F CF₃ C₂H₅ D-448 Cl CF₃ C₂H₅ D-449 Br CF₃ C₂H₅ D-450 CH₃ CF₃ C₂H₅ D-451 C₂H₅ CF₃ C₂H₅ D-452 n-C₃H₇ CF₃ C₂H₅ D-453 i-C₃H₇ CF₃ C₂H₅ D-454 CF₃ CF₃ C₂H₅ D-455 CHF₂ CF₃ C₂H₅ D-456 H H i-C₃H₇ D-457 F H i-C₃H₇ D-458 Cl H i-C₃H₇ D-459 Br H i-C₃H₇ D-460 CH₃ H i-C₃H₇ D-461 C₂H₅ H i-C₃H₇ D-462 n-C₃H₇ H i-C₃H₇ D-463 i-C₃H₇ H i-C₃H₇ D-464 CF₃ H i-C₃H₇ D-465 H F i-C₃H₇ D-466 F F i-C₃H₇ D-467 Cl F i-C₃H₇ D-468 Br F i-C₃H₇ D-469 CH₃ F i-C₃H₇ D-470 C₂H₅ F i-C₃H₇ D-471 n-C₃H₇ F i-C₃H₇ D-472 i-C₃H₇ F i-C₃H₇ D-473 CF₃ F i-C₃H₇ D-474 H Cl i-C₃H₇ D-475 F Cl i-C_(3H) ₇ D-476 Cl Cl i-C₃H₇ D-477 Br Cl i-C₃H₇ D-478 CH₃ Cl i-C₃H₇ D-479 C₂H₅ Cl i-C₃H₇ D-480 n-C₃H₇ Cl i-C₃H₇ D-481 i-C₃H₇ Cl i-C₃H₇ D-482 CF₃ Cl i-C₃H₇ D-483 H Br i-C₃H₇ D-484 F Br i-C₃H₇ D-485 Cl Br i-C₃H₇ D-486 Br Br i-C₃H₇ D-487 CH₃ Br i-C₃H₇ D-488 C₂H₅ Br i-C₃H₇ D-489 n-C₃H₇ Br i-C₃H₇ D-490 i-C₃H₇ Br i-C₃H₇ D-491 CF₃ Br i-C₃H₇ D-492 H CH₃ i-C₃H₇ D-493 F CH₃ i-C₃H₇ D-494 Cl CH₃ i-C₃H₇ D-495 Br CH₃ i-C₃H₇ D-496 CH₃ CH₃ i-C₃H₇ D-497 C₂H₅ CH₃ i-C₃H₇ D-498 n-C₃H₇ CH₃ i-C₃H₇ D-499 i-C₃H₇ CH₃ i-C₃H₇ D-500 CF₃ CH₃ i-C₃H₇ D-501 H C₂H₅ i-C₃H₇ D-502 F C₂H₅ i-C₃H₇ D-503 Cl C₂H₅ i-C₃H₇ D-504 Br C₂H₅ i-C₃H₇ D-505 CH₃ C₂H₅ i-C₃H₇ D-506 C₂H₅ C₂H₅ i-C₃H₇ D-507 n-C₃H₇ C₂H₅ i-C₃H₇ D-508 i-C₃H₇ C₂H₅ i-C₃H₇ D-509 CF₃ C₂H₅ i-C₃H₇ D-510 H i-C₃H₇ i-C₃H₇ D-511 F i-C₃H₇ i-C₃H₇ D-512 Cl i-C₃H₇ i-C₃H₇ D-513 Br i-C₃H₇ i-C₃H₇ D-514 CH₃ i-C₃H₇ i-C₃H₇ D-515 C₂H₅ i-C₃H₇ i-C₃H₇ D-516 n-C₃H₇ i-C₃H₇ i-C₃H₇ D-517 i-C₃H₇ i-C₃H₇ i-C₃H₇ D-518 CF₃ i-C₃H₇ i-C₃H₇ D-519 CHF₂ i-C₃H₇ i-C₃H₇ D-520 CH₂F i-C₃H₇ i-C₃H₇ D-521 H CF₃ i-C₃H₇ D-522 F CF₃ i-C₃H₇ D-523 Cl CF₃ i-C₃H₇ D-524 Br CF₃ i-C₃H₇ D-525 CH₃ CF₃ i-C₃H₇ D-526 C₂H₅ CF₃ i-C₃H₇ D-527 n-C₃H₇ CF₃ i-C₃H₇ D-528 i-C₃H₇ CF₃ i-C₃H₇ D-529 CF₃ CF₃ i-C₃H₇ D-530 CHF₂ CF₃ i-C₃H₇

The compounds I are suitable as fungicides. They are distinguished by outstanding activity against a broad spectrum of phytopathogenic fungi, in particular from the classes of the Ascomycetes, Deuteromycetes, Phycomycetes and Basidiomycetes. Some of them act systemically, and they can be employed in crop protection as foliar- and soil-acting fungicides.

They are especially important for controlling a large number of fungi on a variety of crop plants such as wheat, rye, barley, oats, rice, maize, grass, bananas, cotton, soya, coffee, sugar cane, grapevines, fruit species, ornamentals and vegetables such as cucumbers, beans, tomatoes, potatoes and cucurbits, and on the seeds of these plants.

Specifically, they are suitable for controlling the following plant diseases:

Alternaria species on vegetables and fruit,

Botrytis cinerea (gray mold) on strawberries, vegetables, ornamentals and grapevines,

Cercospora arachidicola on peanuts,

Erysiphe cichoracearum and Sphaerotheca fuliginea on cucurbits,

Erysiphe graminis (powdery mildew) on cereals,

Fusarium and Verticillium species on various plants,

Helminthosporium species on cereals,

Mycosphaerella species on bananas and peanuts,

Phytophthora infestans on potatoes and tomatoes,

Plasmopara viticola on grapevines,

Podosphaera leucotricha on apples,

Pseudocercosporella herpotrichoides on wheat and barley,

Pseudocercosporella species on hops and cucumbers,

Puccinia species on cereals,

Pyricularia oryzae on rice,

Rhizoctonia species on cotton, rice and lawns,

Septoria nodorum on wheat,

Uncinula necator on grapevines,

Ustilago species on cereals and sugar cane, and

Venturia inaequalis (scab) on apples and pears.

Moreover, the compounds I are suitable for controlling harmful fungi such as Paecilomyces variotii in the protection of materials (eg. wood, paper, paint dispersions, fibers and tissues) and in the protection of stored products.

The compounds I are applied by treating the fungi, or the plants, seeds, materials or the soil to be protected against fungal infection, with a fungicidally active amount of the active ingredients. Application can be effected both before and after infection of the materials, plants or seeds by the fungi.

In general, the fungicidal compositions comprise from 0.1 to 95, preferably 0.5 to 90%, by weight of active ingredient.

When used in crop protection, the rates of application are from 0.01 to 2.0 kg of active ingredient per ha, depending on the nature of the effect desired.

In the treatment of seed, amounts of active ingredient of from 0.001 to 0.1 g, preferably 0.01 to 0.05 g, are generally required per kilogram of seed.

When used in the protection of materials or stored products, the rate of application of active ingredient depends on the nature of the field of application and on the effect desired. Rates of application conventionally used in the protection of materials are, for example, from 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of active ingredient per cubic meter of material treated.

Moreover, the compounds of the formula I are suitable for efficiently controlling animal pests from the classes of the insects, arachnids and nematodes. They can be employed in crop protection and in the hygiene, stored-product and veterinary sector for controlling animal pests. In particular, they are suitable for controlling the following animal pests:

insects from the order of the lepidopterans (Lepidoptera), for example Agrotis ypsilon, Agrotis segetum, Alabama argillacea, Anticarsia gemmatalis, Argyresthia conjugella, Autographa gamma, Bupalus piniarius, Cacoecia murinana, Capua reticulana, Cheimatobia brumata, Choristoneura fumiferana, Choristoneura occidentalis, Cirphis unipuncta, Cydia pomonella, Dendrolimus pini, Diaphania nitidalis, Diatraea grandiosella, Earias insulana, Elasmopalpus lignosellus, Eupoecilia ambiguella, Evetria bouliana, Feltia subterranea, Galleria mellonella, Grapholitha funebrana, Grapholitha molesta, Heliothis armigera, Heliothis virescens, Heliothis zea, Hellula undalis, Hibernia defoliaria, Hyphantria cunea, Hyponomeuta malinellus, Keiferia lycopersicella, Lambdina fiscellaria, Laphygma exigua, Leucoptera coffeella, Leucoptera scitella, Lithocolletis blancardella, Lobesia botrana, Loxostege sticticalis, Lymantria dispar, Lymantria monacha, Lyonetia clerkella, Malacosoma neustria, Mamestra brassicae, Orgyia pseudotsugata, Ostrinia nubilalis, Panolis flammea, Pectinophora gossypiella, Peridroma saucia, Phalera bucephala, Phthorimaea operculella, Phyllocnistis citrella, Pieris brassicae, Plathypena scabra, Plutella xylostella, Pseudoplusia includens, Rhyacionia frustrana, Scrobipalpula absoluta, Sitotroga cerealella, Sparganothis pilleriana, Spodoptera frugiperda, Spodoptera littoralis, Spodoptera litura, Thaumatopoea pityocampa, Tortrix viridana, Trichoplusia ni and Zeiraphera canadensis,

beetles (Coleoptera), for example Agrilus sinuatus, Agriotes lineatus, Agriotes obscurus, Amphimallus solstitialis, Anisandrus dispar, Anthonomus grandis, Anthonomus pomorum, Atomaria linearis, Blastophagus piniperda, Blitophaga undata, Bruchus rufimanus, Bruchus pisorum, Bruchus lentis, Byctiscus betulae, Cassida nebulosa, Cerotoma trifurcata, Ceuthorrhynchus assimilis, Ceuthorrhynchus napi, Chaetocnema tibialis, Conoderus vespertinus, Crioceris asparagi, Diabrotica longicornis, Diabrotica 12-punctata, Diabrotica virgifera, Epilachna varivestis, Epitrix hirtipennis, Eutinobothrus brasiliensis, Hylobius abietis, Hypera brunneipennis, Hypera postica, Ips typographus, Lema bilineata, Lema melanopus, Leptinotarsa decemlineata, Limonius californicus, Lissorhoptrus oryzophilus, Melanotus communis, Meligethes aeneus, Melolontha hippocastani, Melolontha melolontha, Oulema oryzae, Otiorrhynchus sulcatus, Otiorrhynchus ovatus, Phaedon cochleariae, Phyllotreta chrysocephala, Phyllophaga sp., Phyllopertha horticola, Phyllotreta nemorum, Phyllotreta striolata, Popillia japonica, Sitona lineatus and Sitophilus granaria,

dipterans (Diptera), for example Aedes aegypti, Aedes vexans, Anastrepha ludens, Anopheles maculipennis, Ceratitis capitata, Chrysomya bezziana, Chrysomya hominivorax, Chrysomya macellaria, Contarinia sorghicola, Cordylobia anthropophaga, Culex pipiens, Dacus cucurbitae, Dacus oleae, Dasineura brassicae, Fannia canicularis, Gasterophilus intestinalis, Glossina morsitans, Haematobia irritans, Haplodiplosis equestris, Hylemyia platura, Hypoderma lineata, Liriomyza sativae, Liriomyza trifolii, Lucilia cuprina, Lucilia sericata, Lycoria pectoralis, Mayetiola destructor, Musca domestica, Muscina stabulans, Oestrus ovis, Oscinella frit, Pegomya hysocyami, Phorbia antiqua, Phorbia brassicae, Phorbia coarctata, Rhagoletis cerasi, Rhagoletis pomonella, Tabanus bovinus, Tipula oleracea and Tipula paludosa, thrips (Thysanoptera), eg. Frankliniella fusca, Frankliniella occidentalis, Frankliniella tritici, Scirtothrips citri, Thrips oryzae, Thrips palmi and Thrips tabaci, hymenopterans (Hymenoptera), eg. Athalia rosae, Atta cephalotes, Atta sexdens, Atta texana, Hoplocampa minuta, Hoplocampa testudinea, Monomorium pharaonis, Solenopsis geminata and Solenopsis invicta,

heteropterans (Heteroptera), eg. Acrosternum hilare, Blissus leucopterus, Cyrtopeltis notatus, Dysdercus cingulatus, Dysdercus intermedius, Eurygaster integriceps, Euschistus impictiventris, Leptoglossus phyllopus, Lygus lineolaris, Lygus pratensis, Nezara viridula, Piesma quadrata, Solubea insularis and Thyanta perditor,

homopterans (Homoptera), eg. Acyrthosiphon onobrychis, Adelges laricis, Aphidula nasturtii, Aphis fabae, Aphis pomi, Aphis sambuci, Brachycaudus cardui, Brevicoryne brassicae, Cerosipha gossypii, Dreyfusia nordmannianae, Dreyfusia piceae, Dysaphis radicola, Dysaulacorthum pseudosolani, Empoasca fabae, Macrosiphum avenae, Macrosiphum euphorbiae, Macrosiphon rosae, Megoura viciae, Metopolophium dirhodum, Myzodes persicae, Myzus cerasi, Nilaparvata lugens, Pemphigus bursarius, Perkinsiella saccharicida, Phorodon humuli, Psylla mali, Psylla piri, Rhopalomyzus ascalonicus, Rhopalosiphum maidis, Sappaphis mala, Sappaphis mali, Schizaphis graminum, Schizoneura lanuginosa, Trialeurodes vaporariorum and Viteus vitifolii,

termites (Isoptera), eg. Calotermes flavicollis, Leucotermes flavipes, Reticulitermes lucifugus und Termes natalensis,

orthopterans (Orthoptera), eg. Acheta domestica, Blatta orientalis, Blattella germanica, Forficula auricularia, Gryllotalpa gryllotalpa, Locusta migratoria, Melanoplus bivittatus, Melanoplus femur-rubrum, Melanoplus mexicanus, Melanoplus sanguinipes, Melanoplus spretus, Nomadacris septemfasciata, Periplaneta americana, Schistocerca americana, Schistocerca peregrina, Stauronotus maroccanus and Tachycines asynamorus,

Arachnoidea, such as arachnids (Acarina), eg. Amblyomma americanum, Amblyomma variegatum, Argas persicus, Boophilus annulatus, Boophilus decoloratus, Boophilus microplus, Brevipalpus phoenicis, Bryobia praetiosa, Dermacentor silvarum, Eotetranychus carpini, Eriophyes sheldoni, Hyalomma truncatum, Ixodes ricinus, Ixodes rubicundus, Ornithodorus moubata, Otobius megnini, Paratetranychus pilosus, Dermanyssus gallinae, Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes ovis, Rhipicephalus appendiculatus, Rhipicephalus evertsi, Sarcoptes scabiei, Tetranychus cinnabarinus, Tetranychus kanzawai, Tetranychus pacificus, Tetranychus telarius and Tetranychus urticae,

nematodes such as root knot nematodes, eg. Meloidogyne hapla, Meloidogyne incognita, Meloidogyne javanica, cyst-forming nematodes, eg. Globodera rostochiensis, Heterodera avenae, Heterodera glycines, Heterodera schachtii, Heterodera trifolii, stem eelworms and foliar nematodes, eg. Belonolaimus longicaudatus, Ditylenchus destructor, Ditylenchus dipsaci, Heliocotylenchus multicinctus, Longidorus elongatus, Radopholus similis, Rotylenchus robustus, Trichodorus primitivus, Tylenchorhynchus claytoni, Tylenchorhynchus dubius, Pratylenchus neglectus, Pratylenchus penetrans, Pratylenchus curvitatus and Pratylenchus goodeyi.

The rate of application of active ingredient for controlling animal pests is from 0.1 to 2.0, preferably 0.2 to 1.0, kg/ha under field conditions.

The compounds I can be converted into the customary formulations, eg. solutions, emulsions, suspensions, dusts, powders, pastes and granules. The use form depends on the particular purpose; in any case, it should ensure a fine and uniform distribution of the compound according to the invention.

The formulations are prepared in a known manner, eg. by extending the active ingredient with solvents and/or carriers, if desired using emulsifiers and dispersants, it also being possible to use other organic solvents as auxiliary solvents if water is used as the diluent. Auxiliaries which are suitable are essentially: solvents such as aromatics (eg. xylene), chlorinated aromatics (eg. chlorobenzenes), paraffins (eg. mineral oil fractions), alcohols (eg. methanol, butanol), ketones (eg. cyclohexanone), amines (eg. ethanolamine, dimethylformamide) and water; carriers such as ground natural minerals (eg. kaolins, clays, talc, chalk) and ground synthetic minerals (eg. highly-disperse silica, silicates); emulsifiers such as non-ionic and anionic emulsifiers (eg. polyoxyethylene fatty alcohol ethers, alkylsulfonates and arylsulfonates) and dispersants such as lignin-sulfite waste liquors and methylcellulose.

Suitable surfactants are alkali metal, alkaline earth metal and ammonium salts of lignosulfonic acid, naphthalenesulfonic acid, phenolsulfonic acid, dibutylnaphthalenesulfonic acid, alkylarylsulfonates, alkyl sulfates, alkylsulfonates, fatty alcohol sulfates and fatty acids and their alkali metal and alkaline earth metal salts, salts of sulfated fatty alcohol glycol ether, condensates of sulfonated naphthalene and naphthalene derivatives with formaldehyde, condensates of naphthalene or of napthalenesulfonic acid with phenol or formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctylphenol, octylphenol, nonylphenol, alkylphenol polyglycol ethers, tributylphenyl polyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol/ethylene oxide condensates, ethoxylated castor oil, polyoxyethylene alkyl ethers, ethoxylated polyoxypropylene, lauryl alcohol polyglycol ether acetal, sorbitol esters, lignin-sulfite waste liquors and methylcellulose.

Substances which are suitable for the preparation of directly sprayable solutions, emulsions, pastes or oil dispersions are mineral oil fractions of medium to high boiling point, such as kerosene or diesel oil, furthermore coal tar oils and oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, eg. benzene, toluene, xylene, paraffin, tetrahydro-naphthalene, alkylated naphthalenes or their derivatives, methanol, ethanol, propanol, butanol, chloroform, carbon tetrachloride, cyclohexanol, cyclohexanone, chlorobenzene, isophorone, strongly polar solvents, eg. dimethylformamide, dimethyl sulfoxide, N-methylpyrrolidone and water.

Powders, materials for spreading and dusts can be prepared by mixing or concomitantly grinding the active substances with a solid carrier.

Granules, eg. coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers. Examples of solid carriers are mineral earths, such as silicas, silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, fertilizers, eg. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders and other solid carriers.

In general, the formulations comprise from 0.01 to 95% by weight, preferably from 0.1 to 90% by weight, of the active ingredient. The active ingredients are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).

The following are exemplary formulations:

I. 5 parts by weight of a compound according to the invention are mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dust which comprises 5% by weight of the active ingredient.

II. 30 parts by weight of a compound according to the invention are mixed intimately with a mixture of 92 parts by weight of pulverulent silica gel and 8 parts by weight of paraffin oil which had been sprayed onto the surface of this silica gel.

This gives a formulation of the active ingredient with good adhesion properties (comprises 23% by weight of active ingredient).

III. 10 parts by weight of a compound according to the invention are dissolved in a mixture composed of 90 parts by weight of xylene, 6 parts by weight of the adduct of 8 to 10 mol of ethylene oxide and 1 mol of oleic acid N-monoethanolamide, 2 parts by weight of calcium dodecylbenzenesulfonate and 2 parts by weight of the adduct of 40 mol of ethylene oxide and 1 mol of castor oil (comprises 9% by weight of active ingredient).

IV. 20 parts by weight of a compound according to the invention are dissolved in a mixture composed of 60 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 5 parts by weight of the adduct of 7 mol of ethylene oxide and 1 mol of isooctylphenol and 5 parts by weight of the adduct of 40 mol of ethylene oxide and 1 mol of castor oil (comprises 16% by weight of active ingredient).

V. 80 parts by weight of a compound according to the invention are mixed thoroughly with 3 parts by weight of sodium diisobutylnaphthalene-alpha-sulfonate, 10 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 7 parts by weight of pulverulent silica gel, and the mixture is ground in a hammer mill (comprises 80% by weight of active ingredient).

VI. 90 parts by weight of a compound according to the invention are mixed with 10 parts by weight of N-methyl-a-pyrrolidone, which gives a solution which is suitable for use in the form of microdrops (comprises 90% by weight of active ingredient).

VII. 20 parts by weight of a compound according to the invention are dissolved in a mixture composed of 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of the adduct of 7 mol of ethylene oxide and 1 mol of isooctylphenol and 10 parts by weight of the adduct of 40 mol of ethylene oxide and 1 mol of castor oil. Pouring the solution into 100,000 parts by weight of water and finely distributing it therein gives an aqueous dispersion which comprises 0.02% by weight of the active ingredient.

VIII. 20 parts by weight of a compound according to the invention are mixed thoroughly with 3 parts by weight of sodium diisobutylnaphthalene-α-sulfonate, 17 parts by weight of the sodium salt of a lignosulfonic acid from a sulfite waste liquor and 60 parts by weight of pulverulent silica gel, and the mixture is ground in a hammer mill. Finely distributing the mixture in 20,000 parts by weight of water gives a spray mixture which comprises 0.1% by weight of the active ingredient.

The active ingredients can be used as such, in the form of their formulations or the use forms prepared therefrom, eg. in the form of directly sprayable solutions, powders, suspensions or dispersions, emulsions, oil dispersions, pastes, dusts, materials for spreading or granules, by means of spraying, atomizing, dusting, spreading or pouring. The use forms depend entirely on the intended purposes; in any case, they are intended to guarantee the finest possible distribution of the active ingredients according to the invention.

Aqueous use forms can be prepared from emulsion concentrates, pastes or wettable powders (sprayable powders, oil dispersions) by adding water. To prepare emulsions, pastes or oil dispersions, the substances as such, or dissolved in an oil or solvent, can be homogenized in water by means of a wetting agent, tackifier, dispersant or emulsifier. Alternatively, it is possible to prepare concentrates composed of an active substance, wetter, tackifier, dispersant or emulsifier and, if appropriate, solvent or oil, and such concentrates are suitable for dilution with water.

The active ingredient concentrations in the ready-to-use products can be varied within substantial ranges. In general, they are from 0.0001 to 10%, preferably from 0.01 to 1%.

The active ingredients may also be used successfully in the ultra-low-volume process (ULV), it being possible to apply formulations comprising over 95% by weight of active ingredient, or even the active ingredient without additives.

Various types of oils, herbicides, fungicides, other pesticides or bactericides may be added to the active ingredients, if appropriate also only immediately prior to use (tank mix). These agents can be admixed with the agents according to the invention 45 in a weight ratio of 1:10 to 10:1.

In the use form as fungicides, the compositions according to the invention can also be present together with other active ingredients, eg. with herbicides, insecticides, growth regulators, fungicides or else with fertilizers. Mixing the compounds I or the compositions comprising them in the use form as fungicides with other fungicides frequently results in a broader fungicidal spectrum of action.

The following list of fungicides together with which the compounds according to the invention can be used is intended to illustrate the possible combinations, but not to impose any limitation:

sulfur, dithiocarbamates and their derivatives, such as iron (III) dimethyldithiocarbamate, zinc dimethyldithiocarbamate, zinc ethylenebisdithiocarbamate, manganese ethylenebisdithiocarbamate, manganese zinc ethylenediamine-bisdithiocarbamate, tetramethylthiuram disulfide, ammonia complex of zinc (N,N-ethylenebisdithiocarbamate), ammonia complex of zinc (N,N′-propylenebisdithiocarbamate), zinc (N,N′-propylenebisdithiocarbamate), N,N′-polypropylenebis(thiocarbamoyl)disulfide;

nitro derivatives, such as dinitro-(1-methylheptyl)phenyl crotonate, 2-sec-butyl-4,6-dinitrophenyl 3,3-dimethylacrylate, 2-sec-butyl-4,6-dinitrophenylisopropyl carbonate, diisopropyl 5-nitro-isophthalate;

heterocyclic substances, such as 2-heptadecyl-2-imidazoline acetate, 2,4-dichloro-6-(o-chloroanilino)-s-triazine, O,O-diethyl phthalimidophosphonothioate, 5-amino-1-[bis-(dimethylamino)phosphinyl]-3-phenyl-1,2,4-triazole, 2,3-dicyano-1,4-dithioanthraquinone, 2-thio-1,3-dithiolo-[4,5-b]quinoxaline, methyl 1-(butylcarbamoyl)-2-benzimidazole-carbamate, 2-methoxycarbonylaminobenzimidazole, 2-(2-furyl)-benzimidazole, 2-(4-thiazolyl)benzimidazole, N-(1,1,2,2-tetrachloroethylthio)tetrahydrophthalimide, N-trichloromethylthio-tetrahydrophthalimide, N-trichloromethylthiophthalimide,

N-dichlorofluoromethylthio-N′,N′-dimethyl-N-phenylsulfodiamide, 5-ethoxy-3-trichloromethyl-1,2,3-thiadiazole, 2-thiocyanatomethylthiobenzothiazole, 1,4-dichloro-2,5-dimethoxy-benzene, 4-(2-chlorophenylhydrazono)-3-methyl-5-isoxazolone, pyridine-2-thiol 1-oxide, 8-hydroxyquinoline or its copper salt, 2,3-dihydro-5-carboxanilido-6-methyl-1,4-oxathiine, 2,3-dihydro-5-carboxanilido-6-methyl-1,4-oxathiine 4,4-dioxide, 2-methyl-5,6-dihydro-4H pyran-3-carboxanilide, 2-methylfuran-3-carboxanilide, 2,5-dimethylfuran-3-carboxanilide, 2,4,5-tri-methylfuran-3-carboxanilide, N-cyclohexyl-2,5-dimethylfuran-3-carboxamide, N-cyclohexyl-N-methoxy-2,5-dimethylfuran-3-carboxamide, 2-methylbenzanilide, 2-iodobenzanilide, N-formyl-N-morpholine-2,2,2-trichloroethyl acetal, piperazine-1,4-diylbis-1-(2,2,2-trichloroethyl)formamide, 1-(3,4-dichloroanilino)-1-formylamino-2,2,2-trichlorethane, 2,6-dimethyl-N-tridecylmorpholine or its salts, 2,6-dimethyl-N-cyclododecylmorpholine or its salts, N-[3-(p-tert-butyl-phenyl)-2-methylpropyl]-cis-2,6-dimethylmorpholine, N-[3-(p-tert-butylphenyl)-2-methylpropyl]piperidine, 1-[2-(2,4-dichlorophenyl)-4-ethyl-1,3-dioxolan-2-ylethyl]-1H 1,2,4-triazole, 1-[2-(2,4-dichlorophenyl)-4-n-propyl-1,3-dioxolan-2-ylethyl]-1H 1,2,4-triazole, N-(n-propyl)-N-(2,4,6-trichlorophenoxyethyl)-N′-imidazolylurea, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H 1,2,4-triazol-1-yl)-2-butanone, 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol, (2RS,3RS)-1-[3-(2-chlorophenyl)-2-(4-fluorophenyl)oxiran-2-ylmethyl]-1H-1,2,4-triazole, α-(2-chlorophenyl)-α-(4-chlorophenyl)-5-pyrimidinemethanol, 5-butyl-2-dimethylamino-4-hydroxy-6-methylpyrimidine, bis(p-chlorophenyl)-3-pyridinemethanol, 1,2-bis(3-ethoxycarbonyl-2-thioureido)benzene, 1,2-bis(3-methoxycarbonyl-2-thioureido)benzene,

strobilurines such as methyl E-methoxyimino-[α-(o-tolyloxy)-o-tolyl]acetate, methyl E-2-{2-[6-(2-cyanophenoxy)pyrimidin-4-yloxy]phenyl}-3-methoxyacrylate, methyl-E-methoxyimino-[α-(2-phenoxyphenyl)]acetamide, methyl E-methoxyimino-[α-(2,5-dimethylphenoxy)-o-tolyl]acetamide,

anilinopyrimidines such as N-(4,6-dimethylpyrimidin-2-yl)aniline, N-[4-methyl-6-(1-propynyl)pyrimidin-2-yl]aniline, N-[4-methyl-6-cyclopropylpyrimidin-2-yl]aniline,

phenylpyrroles such as 4-(2,2-difluoro-1,3-benzodioxol-4-yl)-pyrrole-3-carbonitrile,

cinnamamides such as 3-(4-chlorophenyl)-3-(3,4-dimethoxy-phenyl)acryloylmorpholide,

and a variety of fungicides such as dodecylguanidine acetate, 3-[3-(3,5-dimethyl-2-oxycyclohexyl)-2-hydroxyethyl]glutarimide, hexachlorobenzene, methyl N-(2,6-dimethylphenyl)-N-(2-furoyl)-DL-alaninate, DL-N-(2,6-dimethylphenyl)-N-(2′-methoxyacetyl)alanine methyl ester, N-(2,6-dimethylphenyl)-N-chloroacetyl-D,L-2-aminobutyrolactone, DL-N-(2,6-dimethylphenyl)-N-(phenylacetyl)alanine methyl ester, 5-methyl-5-vinyl-3-(3,5-dichlorophenyl)-2,4-dioxo-1,3-oxazolidine, 3-(3,5-dichlorophenyl)-5-methyl-5-methoxymethyl-1,3-oxazolidine-2,4-dione, 3-(3,5-dichlorophenyl)-1-isopropyl-carbamoylhydantoin, N-(3,5-dichlorophenyl)-1,2-dimethyl-cyclopropane-1,2-dicarboximide, 2-cyano-[N-(ethyl-aminocarbonyl)-2-methoximino]acetamide, 1-[2-(2,4-dichlorophenyl)pentyl]-1H-1,2,4-triazole, 2,4-difluoro-α-(1H-1,2,4-triazolyl-1-methyl)benzhydryl alcohol, N-(3-chloro-2,6-dinitro-4-trifluoromethylphenyl)-5-trifluoromethyl-3-chloro-2-amino-pyridine, 1-((bis(4-fluorophenyl)methylsilyl)methyl)-1H-1,2,4-triazole.

SYNTHESIS EXAMPLES

With due modification of the starting compounds, the protocols shown in the synthesis examples below were used for obtaining further compounds I. The resulting compounds, together with physical data, are listed in the Tables which follow.

Example 1 Preparation of 2-chloro-4-(3,5-dimethylpyrazol-1-yl)phenol

At from −5 to −10° C., a suspension of 123 g (858 mmol) of 2-chloro-4-aminophenol in 190 ml of conc. HCl was added dropwise to a solution of 71 g (1 mol) of NaNO₂ in 190 ml of water. At from −5 to −10° C., this suspension was added to a solution of 354 g (1.72 mol) of SnCl₂*2H₂O in 800 ml of conc. HCl. The mixture was stirred at about 20-25° C. for approximately 14 hours and the crystalline material was filtered off and washed with water. After drying, 85 g of 3-chloro-4-hydroxyphenyldiazonium hydrochloride were obtained.

A suspension of 39 g (0.2 mol) of the diazonium salt in 200 ml of ethanol was admixed with 17 g (0.2 mol) of acetylacetone and the mixture was refluxed for two hours. The solvent was distilled off and the residue was then digested in a water/methylene chloride mixture. The crystalline material was filtered off and then washed with methylene chloride, giving 17 g of the title compound as HCl salt.

Example 2 Preparation of methyl 2-{2-chloro-[4-(3,5-dimethyl)-pyrazol-1-yl]phenoxymethylene}phenylglyoxylate O-methyloxime [I-12]

A solution of 1.2 g (5 mmol) of the phenylpyrazole from Example 1, 1.6 g (5 mmol) of methyl 2-bromomethylphenylglyoxylate O-methyloxime [cf. EP-A 254 426] and 2.2 g (16 mmol) of potassium carbonate in 30 ml of dimethylformamide (DMF) was stirred at 20-25° C. for approximately 14 hours. The reaction mixture was taken up in water and extracted with methyl tert-butyl ether (MTBE). The combined organic phases were washed with water and dried. The solvent was distilled off and the residue was chromatographed over silica gel (cyclohexane/ethyl acetate 1:1), giving 1.7 g of the title compound in the form of colorless crystals.

Example 3 Preparation of N-methyl-2-{2-chloro-[4-(3,5-dimethyl)pyrazol-1-yl]phenoxymethylene}-phenylglyoxamide O-methyloxime [I-11]

A solution of 1.7 g (4 mmol) of the ester II-12 and 1 ml of 40% strength aqueous methylamine solution were dissolved in 25 ml of tetrahydrofuran and the mixture was stirred at 20-25° C. for about 3.5 hours. The solvent was distilled off and the residue was crystallized from diisopropyl ether, giving 1.3 g of the title compound.

Example 4 Preparation of 1-methyl-4-{ortho-[2-chloro-4-(3,5-dimethylpyrazol-1-yl)phenoxymethylene]phenyl}-tetrazol-5-one [II-1]

0.12 g of sodium hydride was added to a solution of 1.02 g (4.6 mmol) of 2-chloro-4-(3,5-dimethylpyrazol-1-yl)phenol in 25 ml of anhydrous dimethylformamide. The mixture was stirred at 20-25° C. for 1 hour, after which a solution of 1.24 g of 1-methyl-4-(orthobromomethylene)phenyltetrazol-5-one in 10 ml of anhydrous dimethylformamide was added, and stirring was continued at 20-25° C. for 20 hours. 250 ml of dil. NaCl solution were subsequently added. The mixture was extracted with ethyl acetate, and the organic phase was washed with water, dried and freed of solvents. Recrystallization of the residue from methyl tert-butyl ether/hexane gave 1.3 g of the title compound as light-beige crystals of m.p. 122-124° C.

IR [cm⁻¹]: 1737, 1510, 1457, 1427, 1396, 1282, 1242, 1063, 1031, 747.

Example 5 Preparation of 1-methyl-4-[ortho-(4-iodo-2-methylphenoxymethylene)phenyl]tetrazol-5-one

A solution of 5.38 g (20 mmol) of 1-methyl-4-(orthobromomethylene)phenyltetrazol-5-one, 4.68 g (20 mmol) of 4-iodo-2-methylphenol and 4.14 g (60 mmol) of potassium carbonate in 60 ml of anhydrous dimethylformamide was stirred at approximately 85° C. for 4 hours. 600 ml of dil. sodium chloride solution were subsequently added. The reaction solution was extracted with ethyl acetate and the organic phase was washed with water, dried and freed of the solvent. This gave 8.2 g of the title compound as colorless crystals of m.p. 128-130° C.

Example 6 Preparation of 1-methyl-4-(ortho-(2-methyl-4-(1-phenylpyrazol-4-yl)-phenoxymethylene)phenyl)-tetrazol-5-one [II-9]

A solution of 1.48 g (3.5 mmol) of the tetrazolone from Example 5, 1.51 g of (1-phenylpyrazol-4-yl)tributylstannane and 0.2 g of tetrakis(triphenylphosphine)palladium(0) in 20 ml of anhydrous toluene was stirred at 70° C. for 2 hours and then refluxed for 2 hours. The solvent was distilled off and the residue was chromatographed over silica gel (cyclohexane:methyl tert-butyl ether mixture 1:1), giving 0.24 g of the title compound of m.p. 152-153° C.

IR [cm⁻¹]: 1717, 1498, 1411, 1245, 1139, 1015, 813, 753.

TABLE I Phys. data Formula (m.p. [° C.]; IR [cm⁻¹]; No. Y_(n) = H Y¹ Y^(1′) X ¹H NMR (CDCl₃) δ [ppm]) I-1 IC Cl H pyrazol-1-yl 1727, 1521, 1503, 1279, 1223, 1069, 1045, 1018 I-2 ID Cl H pyrazol-1-yl 116-118 I-3 IA Cl H pyrazol-1-yl 146-148 I-4 IB Cl H pyrazol-1-yl 117-119 I-5 IE Cl H pyrazol-1-yl 110-114 I-6 ID Cl H 3,5-(CF₃)₂- 110-113 pyrazol-1-yl I-7 IC Cl H 3,5-(CF₃)₂- 103-106 pyrazol-1-yl I-8 IA Cl H 3,5-(CF₃)₂- 129-132 pyrazol-1-yl I-9 IB Cl H 3,5-(CF₃)₂- 1.1; 1.6(d, 3H); 3.7(s, 3H); pyrazol-1-yl 5.0(s, 2H); 6.9-7.5(m, 9H) I-10 IE Cl H 3,5-(CF₃)₂- 104-106 pyrazol-1-yl I-11 ID Cl H 3,5-(CH₃)₂- 1671, 1555, 1410, 1281, pyrazol-1-yl 1260, 1231, 1062, 1037, 978 I-12 IC Cl H 3,5-(CH₃)₂- 1673, 1512, 1285, 1260, pyrazol-1-yl 1233, 1060, 1033, 1017 I-13 IA Cl H 3,5-(CH₃)₂- pyrazol-1-yl  93-96 I-14 IB Cl H 3,5-(CH₃)₂- pyrazol-1-yl  99-103 I-15 IE Cl H 3,5-(CH₃)₂- 1739, 1710, 1456, 1440, pyrazol-1-yl 1335, 1308, 1286, 1258, 1062 I-16 ID Cl H 3,5-(CH₃)₂- 1675, 1509, 1289, 1259, 4-Cl-pyrazol- 1233, 1060, 1033, 1014, 1-yl 984 I-17 IC Cl H 3-CH₃- 121-126 pyrazol-1-yl I-18 ID Cl H 5-CH₃-  84-89 pyrazol-1-yl I-19 IC Cl H 3-CH₃- 113-117 pyrazol-1-yl I-20 IA Cl H 3-CH₃- 127-131 pyrazol-1-yl I-21 IB Cl H 3-CH₃- 114-119 pyrazol-1-yl I-22 IE Cl H 3-CH₃- 108-110 pyrazol-1-yl I-23 IC Cl H 3-CF₃-5-CH₃- 1728, 1508, 1489, 1463, pyrazol-1-yl 1248, 1233, 1179, 1135, 1069, 1019 I-24 ID Cl H 3-CF₃-5-CH₃-  95-98 pyrazol-1-yl I-25 IA Cl H 3-CF₃-5-CH₃- 139-148 pyrazol-1-yl I-26 IB Cl H 3-CF₃-5-CH₃-  79-83 pyrazol-1-yl I-27 IE Cl H 3-CF₃-5-CH₃- 1740, 1508, 1490, 1459, pyrazol-1-yl 1248, 1235, 1179, 1135, 1101 I-28 ID CH₃ H 3,5-(CF₃)₂- 118-121 pyrazol-1-yl I-29 ID CH₃ H pyrazol-1-yl  75-78 I-30 IC CH₃ H pyrazol-1-yl 111-115 I-31 IA CH₃ H pyrazol-1-yl  97-101 I-32 IB CH₃ H pyrazol-1-yl  85-89

TABLE II Formula Phys. data No. (Y_(n) = H) R^(A) R^(B) (Y¹)_(m) ^(*)) X (m.p. [° C.]; IR [cm⁻¹]) II-1 IH — CH₃ 2-Cl 3,5-(CH₃)₂-pyrazol-1-yl cf. Example 4 II-2 IF OCH₃ CH₃ 2-Cl 3,5-(CH₃)₂-pyrazol-1-yl m.p. = 143-144° C. IR: 1733, 1613, 1515, 1474, 1465, 1414, 1314, 1275, 1267, 1062 II-3 IF OCH₃ CH₃ 2-CH₃ pyrazol-1-yl IR: 1722, 1615, 1519, 1504, 1479, 1414, 1393, 1235, 1235, 753, 743 II-4 IF OCH₃ CH₃ 2-CH₃ 5-CH₃-pyrazol-1-yl IR: 1723, 1615, 1531, 1506, 1478, 1458, 1414, 1234, 1049, 974 II-5 IF OCH₃ CH₃ 2-Cl 3,5-(CF₃)₂-pyrazol-1-yl m.p. = 135-137° C. IR: 1735, 1616, 1513, 1480, 1282, 1260, 1235, 1174, 1143, 1107 II-6 IH — CH₃ 2-Cl 3,5-(CF₃)₂-pyrazol-1-yl m.p. = 138-139° C. IR: 1718, 1513, 1281, 1260, 1246, 1236, 1183, 1169, 1133, 1109 II-7 IH — CH₃ 2-CH₃ 3-CF₃-pyrazol-1-yl m.p. = 122-124° C. IR: 1718, 1514, 1390, 1263, 1246, 1176, 1154, 1144, 1113, 752 II-8 IH — CH₃ 3-CH₃ pyrrol-1-yl m.p. = 136-139° C. IR: 1730, 1513, 1501, 1383, 1236, 1165, 1148, 1030, 737, 728 II-9 IH — CH₃ 2-CH₃ 1-phenylpyrazol-4-yl cf. Example 6 II-10 IF OCH₃ CH₃ 2-CH₃ 3-CF₃-pyrazol-1-yl m.p. = 86-88° C. IR: 1722, 1616, 1506, 1480, 1415, 1388, 1258, 1239, 1170, 1133 II-11 IH — CH₃ 2-CH₃ 4-CH₃-oxazol-2-yl m.p. = 152-153° C. IR: 1723, 1617, 1503, 1399, 1348, 1274, 1262, 1252, 1130, 749 II-12 IH — CH₃ 2-CH₃ pyrazol-1-yl m.p. = 150-152° C. IR: 1716, 1522, 1506, 1403, 1258, 1236, 1052, 1038, 758, 748 *)position of (Y¹)_(m) relative to the oxymethylene bridge

Examples for the Action Against Harmful Fungi

The fungicidal action of the compounds of the formula I was demonstrated by the following experiments:

The active ingredients, separately or together, were prepared as a 10% strength emulsion in a mixture of 70% by weight of cyclohexanone, 20% by weight of Nekanil® LN (Lutensol® AP6, wetting agent having emulsifying and dispersant action based on ethoxylated alkylphenols) and 10% by weight of Wettol® EM (nonionic emulsifier based on ethoxylated castor oil) and diluted with water to the desired concentration.

The compounds A and B known from EP-A 280 185 and WO-A 93/15046, respectively, served as comparative active ingredients:

No. known from Q A EP-A 280 185, No. 126 of the table C(═CHCH₃)COOCH₃ B WO-A 93/15046, No. I-8 of Table 8 N(—OCH₃)COOCH₃

Use Example 1

Activity Against Powdery Mildew of Wheat

Leaves of potted wheat seedlings c.v. “Frühgold” were sprayed to runoff point with an aqueous spray liquor which had been prepared using a stock solution of 10% of active ingredient, 63% of cyclohexanone and 27% of emulsifier and, 24 hours after the spray coating had dried on, dusted with spores of powdery mildew of wheat (Erysiphe graminis form a specialis tritici). The test plants were subsequently placed in a greenhouse at 20-24° C. and 60-90% relative atmospheric humidity. After 7 days, the extent of the mildew development was scored visually in % infection of the total leaf area.

In this test, the plants which had been treated with 16 ppm of the active ingredients No. I-2, I-4, I-5, I-6, I-7, I-9, I-10, I-12, I-13, I-15, I-17, I-18, I-22, I-24 and I-27 of Table I showed at most 15% infection, while the plants which had been treated with 16 ppm of the comparative active ingredient A showed 40% infection and the untreated plants 80% infection.

Use Example 2

Activity Against Plasmopara viticola

Leaves of potted grapevines c.v. “Müller-Thurgau” were sprayed to runoff point with an aqueous spray liquor which had been prepared using a stock solution of 10% of active compound, 63% of cyclohexanone and 27% of emulsifier. To be able to assess the persistency of the substances, the plants were, after the spray coating had dried on, kept in a greenhouse for 7 days. Only then were the leaves inoculated with an aqueous zoospore suspension of Plasmopara viticola. The grapevines were then initially kept in a water-vapor-saturated chamber at 24° C. for 48 hours and subsequently kept in a greenhouse at 20-30° C. for 5 days. After this period of time, the plants were once more placed in a humid chamber for 16 hours to accelerate Sporangiophore eruption. The extent of the disease development on the undersides of the leaves was then determined visually.

In this test, the plants which had been treated with 16 ppm of the active ingredients Nos. I-1, I-2, I-3, I-6, I-l1, I-13, I-15, I-18, I-19, I-20 and I-24 of Table I showed at most 15% infection, while the plants which had been treated with 16 ppm of the comparative active ingredient B showed 25% infection and the untreated plants 75% infection.

Use Example 3

Curative Activity Against Puccinia recondita on Wheat (Leaf Rust of Wheat)

Leaves of potted wheat seedlings c.v. “Frühgold” were dusted with leaf rust spores (Puccinia recondite). The pots were then placed for 24 hours into a chamber with high atmospheric humidity (90 to 95%) at 20 to 25° C. During this time, the spores germinated, and the germinal tubes penetrated the leaf tissue. The next day, the infected plants were sprayed to runoff point with an aqueous spray liquor which had been prepared using a stock solution of 10% of active ingredient, 63% of cyclohexanone and 27% of emulsifier. After the spray coating had dried on, the test plants were cultivated for 7 days in a greenhouse at from 20 to 22° C. and a relative atmospheric humidity of 65 to 70%. The extent of rust development on the leaves was then determined.

In this test, the plants which had been treated with 16 ppm of the active ingredients Nos. I-2, I-11, I-12, I-13, I-14, I-15 and I-18 of Table I showed no infection, while the plants which had been treated with 16 ppm of the comparative active ingredient B showed 55% infection and the untreated plants 80% infection.

Use Example 4

Activity Against Pyricularia oryzae (Protective)

Leaves of potted rice seedlings c.v. “Tai-Nong 67” were sprayed to runoff point with an aqueous preparation of active ingredient which had been prepared using a stock solution of 10% of active ingredient, 63% of cyclohexanone and 27% of emulsifier. The next day, the plants were inoculated with an aqueous spore suspension of Pyricularia oryzae. The test plants were subsequently placed for 6 days into controlled-environment cabinets at 22-24° C. and a relative atmospheric humidity of 95-99%. The extent of the disease development on the leaves was then determined visually.

In this test, the plants which had been treated with 16 ppm of the active ingredients Nos. I-1, I-2, I-6, I-7, I-11, I-12, I-13, I-14, I-15, I-17, I-18, I-19, I-20, I-21 and I-22 of Table I showed at most 15% infection, while the plants which had been treated with 16 ppm of the comparative active ingredient A showed 60% infection and the untreated plants 85% infection.

Use Example 5

Activity Against Botrytis cinerea on Bell Pepper Leaves

Bell pepper seedlings c.v. “Neusiedler Ideal Elite” were, after 4 to 5 leaves were well developed, sprayed to runoff point with an aqueous preparation of active ingredient which had been prepared using a stock solution of 10% of active ingredient, 63% of cyclohexanone and 27% of emulsifier. The next day, the treated plants were innoculated with a spore suspension of Botrytis cinerea which contained 1.7×10⁶ spores/ml in a 2% strength aqueus Biomalz solution. The test plants were subsequently placed into controlled-environment cabinets at 22-24° C. and high atmospheric humidity. After 5 days, the extent of the fungal infection on the leaves could be determined visually in %.

In this test, the plants which had been treated with 250 ppm of the active ingredients II-4, II-5 and II-11 showed 10% infection, while the untreated plants showed 80% infection.

Examples of the Action Against Animal Pests

The action of the compounds of the formula I against animal pests was demonstrated by the following experiments:

The active ingredients were formulated

a. as a 0.1% strength solution in acetone or

b. as a 10% strength emulsion in a mixture of 70% by weight of cyclohexanone, 20% by weight of Nekanil® LN (Lutensol® AP6, wetting agent having emulsifying and dispersant action based on ethoxylated alkylphenols) and 10% by weight of Wettol® EM (nonionic emulsifier based on ethoxylated castor oil)

and the formulations were diluted to give the desired concentration, using acetone in the case of a. or water in the case of b..

After the experiments had been concluded, in each case the lowest concentration was determined at which the compounds still caused an 80 to 100% inhibition or mortality in comparison with untreated controls (limit or minimal concentration).

Action Against Tetranycus urticae (Greenhouse Red Spider Mite)

Potted bush beans which showed the second pair of adult leaves were sprayed to runoff point with the aqueous preparation of active ingredient. The plants were strongly infested by adult mites and had eggs deposited on them. After 5 days in a greenhouse, the infestation was determined using a binocular.

In this test, the active ingredient I-9 showed a limit concentration of 100 ppm, while the comparative active ingredient A showed a limit concentration of 400 ppm. 

We claim:
 1. A benzyl phenyl ether of formula I

wherein Q is C(═CHOCH₃)—COOCH₃, C(═CHCH₃)—COOCH₃, C(═NOCH₃)—COOCH₃, C(═NOCH₃)—CONHCH₃ or N(—OCH₃)—COOCH₃; X is pyrazolyl which is unsubstituted or substituted by a group Y² _(p); Y, Y¹ are halogen, cyano, nitro, C₁ 14 C₄-alkyl, C₁ 14 C₄-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl or C₁-C₄-alkoxy; Y² is halogen, cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₂-C₆-alkenyl, C₂-C₆-haloalkenyl, C₂-C₆-alkynyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylamino, di-C₁-C₄-alkylamino or C₁-C₄-alkylthio, or  phenyl, phenoxy or benzyl, where the aromatic rings may be partially or fully halogenated or may carry one to three groups R⁴: R⁴ is halogen, cyano, nitro, hydroxyl, mercapto, amino, carboxyl, aminocarbonyl, aminothiocarbonyl, alkyl, haloalkyl, alkenyl, alkenyloxy, alkynyloxy, alkoxy, haloalkoxy, alkylthio, alkylamino, dialkylamio, formyl, alkylcarbonyl, alkylsulfonyl, alkylsulfoxyl, alkoxycarbonyl, alkylcarbonyloxy, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminothiocarbonyl, dialkylaminothiocarbonyl, where the alkyl groups in these radicals contain 1 to 6 carbon atoms and the abovementioned alkenyl or alkynyl groups in these radicals contain 2 to 8 carbon atoms;  and/or one to three of the following radicals cycloalkyl, cycloalkoxy, heterocyclyl, heterocyclyloxy, where the cyclic systems contain 3 to 10 ring members; aryl, aryloxy, arylthio, aryl-C₁-C₆-alkoxy, aryl-C₁-C₆-alkyl, hetaryl, hetaryloxy, hetarylthio, where the aryl radicals preferably contain 6 to 10 ring members, the hetaryl radicals 5 or 6 ring members, where the cyclic systems may be partially or fully halogenated or may be substituted by one to three groups R⁵ or by one or two groups R⁶: R⁵ is halogen, cyano, nitro, hydroxyl, C₁-C₆-alkyl, C₁-C₆-haloalkyl, C₁-C₆-alkylcarbonyl, C₃-C₆-cycloalkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkoxy, C₁-C₆-alkoxycarbonyl, C₁-C₆-alkylthio, C₁-C₆-alkylamino, di-C₁-C₆-alkylamino, C₂-C₆-alkenyl, C₂-C₆-alkenyloxy, C₃-C₆-alkynyloxy and C₁-C₄-alkylenedioxy which may be halogenated; and R⁶ is C(═NOR^(d))-Γ₁-R^(d′), where R^(d) is hydrogen or C₁-C₆-alkyl, Γ is oxygen, sulfur or NR^(d) and 1 is 0 or 1; m, n are 0, 1 or 2, where the radicals Y and Y¹ may be different if m or n=2; p is 0, 1, 2 or 3, where the radicals Y² may be different if p=2 or 3; with the proviso that if Q is C(═CHOCH₃)—COOCH₃, C(═CHOCH₃)—CONHCH₃ or C(═NOCH₃)—COOCH₃, the index m is 1 or 2; or a salt thereof.
 2. The benzyl phenyl ether of formula I defined in claim 1 which is represented by formula I′


3. The benzyl phenyl ether of formula I defined in claim 1 which is represented by formula I″

wherein Y¹′ is hydrogen.
 4. A process for preparing the benzyl phenyl ether of formula I defined in claim 1, which comprises reacting a phenol of formula II

with a benzyl compound of formula III

wherein L represents a nucleophilically cleavable group.
 5. A composition suitable for controlling animal pests or harmful fungi which comprises a solid or liquid carrier and an effective amount of the benzyl phenyl ether of formula I defined in claim
 1. 6. A method for controlling harmful fungi, which comprises treating the fungi, or materials, plants, soil or seeds to be protected against fungal attack, with an effective amount of the benzyl phenyl ether of formula I defined in claim
 1. 7. A method for controlling animal pests, which comprises treating the animal pests, or materials, plants, soil or seeds to be protected against the pests, with an effective amount of the benzyl phenyl ether of formula I defined in claim
 1. 8. The benzyl phenyl ether of formula I defined in claim 1, wherein Y² is halogen, cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylamino, di-C₁-C₄-alkylamino and C₁-C₄-alkylthio.
 9. The benzyl phenyl ether of formula I′ defined in claim 2, wherein Y² is halogen, cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylamino, di-C₁-C₄-alkylamino and C₁-C₄-alkylthio.
 10. The benzyl phenyl ether of formula I″ defined in claim 4, wherein Y² is halogen, cyano, nitro, C₁-C₄-alkyl, C₁-C₄-haloalkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkoxy, C₁-C₄-alkylamino, di-C₁-C₄-alkylamino and C₁-C₄-alkylthio. 